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ENST00000505435.4:n.939G=
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ENST00000505787.8:n.2823G=
|
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ENST00000509358.7:c.983G=
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ENSP00000420994.3:p.Ser328=
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ENST00000509539.3:c.245G=
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ENSP00000425474.3:p.Ser82=
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ENST00000510895.7:n.1106G=
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ENST00000629193.3:c.869G=
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ENSP00000486535.2:p.Ser290=
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ENST00000681968.1:c.476G=
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ENSP00000508143.1:p.Ser159=
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ENST00000682045.1:c.839G=
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ENSP00000507329.1:p.Ser280=
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ENST00000682214.1:c.590G=
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ENSP00000507336.1:p.Ser197=
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ENST00000682499.1:n.1804G=
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ENST00000682541.1:c.983G=
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ENSP00000507673.1:p.Ser328=
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ENST00000682687.1:c.983G=
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ENSP00000507945.1:p.Ser328=
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ENST00000682727.1:c.983G=
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ENSP00000507393.1:p.Ser328=
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ENST00000682876.1:c.1112G=
|
ENSP00000508389.1:p.Ser371=
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ENST00000683098.1:c.803+3045G=
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ENSP00000507670.1:n.803+3045G=
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ENST00000683258.1:c.*704G=
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ENSP00000507448.1:n.*704G=
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ENST00000683339.1:c.767G=
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ENSP00000507758.1:p.Ser256=
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ENST00000683403.1:c.893G=
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ENSP00000507896.1:p.Ser298=
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ENST00000683429.1:c.590G=
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ENSP00000507697.1:p.Ser197=
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ENST00000683665.1:c.983G=
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ENSP00000507068.1:p.Ser328=
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ENST00000683789.1:c.869G=
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ENSP00000507012.1:p.Ser290=
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ENST00000683847.1:n.827G=
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ENST00000683882.1:c.983G=
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ENSP00000506735.1:p.Ser328=
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ENST00000684024.1:c.*654G=
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ENSP00000507175.1:n.*654G=
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ENST00000684254.1:c.*709G=
|
ENSP00000508001.1:n.*709G=
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ENST00000684310.1:c.165+188G=
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ENSP00000507550.1:n.165+188G=
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ENST00000684530.1:c.245G=
|
ENSP00000507439.1:p.Ser82=
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ENST00000684652.1:n.1985G=
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ENST00000340941.11:c.983G=
MANE Select
|
ENSP00000343657.6:p.Ser328=
|
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ENST00000340941.10:c.983G=
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ENSP00000343657.6:p.Ser328=
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ENST00000505435.3:n.334G=
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ENST00000509358.6:c.983G=
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ENSP00000420994.2:p.Ser328=
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ENST00000509539.2:c.308G=
|
ENSP00000425474.2:p.Ser103=
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ENST00000510895.6:n.597G=
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ENST00000512218.6:c.869G=
|
ENSP00000423202.2:p.Ser290=
|
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|
ENST00000629193.2:c.869G=
|
ENSP00000486535.1:p.Ser290=
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NM_022132.4:c.983G=
|
NP_071415.1:p.Ser328=
|
|
|
XM_005248567.1:c.869G=
|
XP_005248624.1:p.Ser290=
|
|
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XM_011543528.1:c.983G=
|
XP_011541830.1:p.Ser328=
|
|
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XM_011543529.1:c.983G=
|
XP_011541831.1:p.Ser328=
|
|
|
NM_001363147.1:c.869G=
|
NP_001350076.1:p.Ser290=
|
|
|
XM_011543529.2:c.983G=
|
XP_011541831.1:p.Ser328=
|
|
|
XM_017009688.1:c.983G=
|
XP_016865177.1:p.Ser328=
|
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XR_001742172.1:n.1023G=
|
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NM_022132.5:c.983G=
MANE Select
|
NP_071415.1:p.Ser328=
|
|
