ENST00000695850.1:n.788G=
|
|
|
ENST00000695853.1:c.*671G=
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ENSP00000512218.1:n.*671G=
|
|
ENST00000423902.7:c.7612G=
MANE Select
|
ENSP00000392028.1:p.Asp2538=
|
|
ENST00000423902.6:c.7612G=
|
ENSP00000392028.1:p.Asp2538=
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|
ENST00000524602.5:c.1717-1322G=
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ENSP00000437061.1:n.1717-1322G=
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ENST00000531695.1:n.36G=
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|
|
ENST00000618450.1:n.4G=
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|
|
NM_001316690.1:c.1717-1322G=
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NP_001303619.1:n.1717-1322G=
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|
NM_017780.3:c.7612G=
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NP_060250.2:p.Asp2538=
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|
XM_011517553.1:c.7702G=
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XP_011515855.1:p.Asp2568=
|
|
XM_011517554.1:c.7702G=
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XP_011515856.1:p.Asp2568=
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|
XM_011517555.1:c.7699G=
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XP_011515857.1:p.Asp2567=
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|
XM_011517556.1:c.7699-1289G=
|
XP_011515858.1:n.7699-1289G=
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|
XM_011517557.1:c.5689G=
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XP_011515859.1:p.Asp1897=
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|
XM_011517558.1:c.5239G=
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XP_011515860.1:p.Asp1747=
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|
XM_011517559.1:c.4447G=
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XP_011515861.1:p.Asp1483=
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|
XM_011517553.2:c.7702G=
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XP_011515855.1:p.Asp2568=
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|
XM_011517554.3:c.7702G=
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XP_011515856.1:p.Asp2568=
|
|
XM_011517555.2:c.7699G=
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XP_011515857.1:p.Asp2567=
|
|
XM_017013612.1:c.7702G=
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XP_016869101.1:p.Asp2568=
|
|
XM_017013613.1:c.7609G=
|
XP_016869102.1:p.Asp2537=
|
|
NM_017780.4:c.7612G=
MANE Select
|
NP_060250.2:p.Asp2538=
|
|