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ENST00000505435.4:n.914A=
|
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ENST00000505787.8:n.2798A=
|
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|
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ENST00000509358.7:c.958A=
|
ENSP00000420994.3:p.Ile320=
|
|
|
ENST00000509539.3:c.220A=
|
ENSP00000425474.3:p.Ile74=
|
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ENST00000510895.7:n.1081A=
|
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ENST00000629193.3:c.844A=
|
ENSP00000486535.2:p.Ile282=
|
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ENST00000681968.1:c.451A=
|
ENSP00000508143.1:p.Ile151=
|
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ENST00000682045.1:c.814A=
|
ENSP00000507329.1:p.Ile272=
|
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ENST00000682214.1:c.565A=
|
ENSP00000507336.1:p.Ile189=
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ENST00000682499.1:n.1779A=
|
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ENST00000682541.1:c.958A=
|
ENSP00000507673.1:p.Ile320=
|
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ENST00000682687.1:c.958A=
|
ENSP00000507945.1:p.Ile320=
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|
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ENST00000682727.1:c.958A=
|
ENSP00000507393.1:p.Ile320=
|
|
|
ENST00000682876.1:c.1087A=
|
ENSP00000508389.1:p.Ile363=
|
|
|
ENST00000683098.1:c.803+3020A=
|
ENSP00000507670.1:n.803+3020A=
|
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|
ENST00000683258.1:c.*679A=
|
ENSP00000507448.1:n.*679A=
|
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|
ENST00000683339.1:c.742A=
|
ENSP00000507758.1:p.Ile248=
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ENST00000683403.1:c.868A=
|
ENSP00000507896.1:p.Ile290=
|
|
|
ENST00000683429.1:c.565A=
|
ENSP00000507697.1:p.Ile189=
|
|
|
ENST00000683665.1:c.958A=
|
ENSP00000507068.1:p.Ile320=
|
|
|
ENST00000683789.1:c.844A=
|
ENSP00000507012.1:p.Ile282=
|
|
|
ENST00000683847.1:n.802A=
|
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|
ENST00000683882.1:c.958A=
|
ENSP00000506735.1:p.Ile320=
|
|
|
ENST00000684024.1:c.*629A=
|
ENSP00000507175.1:n.*629A=
|
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|
ENST00000684254.1:c.*684A=
|
ENSP00000508001.1:n.*684A=
|
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|
ENST00000684310.1:c.165+163A=
|
ENSP00000507550.1:n.165+163A=
|
|
|
ENST00000684530.1:c.220A=
|
ENSP00000507439.1:p.Ile74=
|
|
|
ENST00000684652.1:n.1960A=
|
|
|
|
ENST00000340941.11:c.958A=
MANE Select
|
ENSP00000343657.6:p.Ile320=
|
|
|
ENST00000340941.10:c.958A=
|
ENSP00000343657.6:p.Ile320=
|
|
|
ENST00000505435.3:n.309A=
|
|
|
|
ENST00000509358.6:c.958A=
|
ENSP00000420994.2:p.Ile320=
|
|
|
ENST00000509539.2:c.283A=
|
ENSP00000425474.2:p.Ile95=
|
|
|
ENST00000510895.6:n.572A=
|
|
|
|
ENST00000512218.6:c.844A=
|
ENSP00000423202.2:p.Ile282=
|
|
|
ENST00000629193.2:c.844A=
|
ENSP00000486535.1:p.Ile282=
|
|
|
NM_022132.4:c.958A=
|
NP_071415.1:p.Ile320=
|
|
|
XM_005248567.1:c.844A=
|
XP_005248624.1:p.Ile282=
|
|
|
XM_011543528.1:c.958A=
|
XP_011541830.1:p.Ile320=
|
|
|
XM_011543529.1:c.958A=
|
XP_011541831.1:p.Ile320=
|
|
|
NM_001363147.1:c.844A=
|
NP_001350076.1:p.Ile282=
|
|
|
XM_011543529.2:c.958A=
|
XP_011541831.1:p.Ile320=
|
|
|
XM_017009688.1:c.958A=
|
XP_016865177.1:p.Ile320=
|
|
|
XR_001742172.1:n.998A=
|
|
|
|
NM_022132.5:c.958A=
MANE Select
|
NP_071415.1:p.Ile320=
|
|
