ENST00000413300.2:c.354A=
|
|
|
ENST00000454293.2:c.832A=
|
ENSP00000412014.2:p.Thr278=
|
|
ENST00000458276.7:c.774-591A=
|
ENSP00000390849.3:n.774-591A=
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|
ENST00000463153.2:c.182A=
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|
|
ENST00000642351.1:c.832A=
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ENSP00000494478.1:p.Thr278=
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ENST00000643140.1:c.*317A=
|
ENSP00000495588.1:n.*317A=
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ENST00000643477.1:c.*416A=
|
ENSP00000496220.1:n.*416A=
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ENST00000643500.1:c.*156A=
|
ENSP00000494735.1:n.*156A=
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ENST00000643520.1:n.1121A=
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ENST00000644371.2:c.955A=
MANE Select
|
ENSP00000495778.1:p.Thr319=
|
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ENST00000646378.1:c.*1005A=
|
ENSP00000495826.1:n.*1005A=
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ENST00000646799.1:c.*248-591A=
|
ENSP00000494829.1:n.*248-591A=
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|
ENST00000649763.1:c.955A=
|
ENSP00000497701.1:p.Thr319=
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|
ENST00000413300.1:c.356A=
|
ENSP00000392159.1:p.Asp119=
|
|
ENST00000458276.6:c.955A=
|
ENSP00000390849.2:p.Thr319=
|
|
ENST00000463153.1:n.185A=
|
|
|
NM_016006.4:c.955A=
|
NP_057090.2:p.Thr319=
|
|
XM_011533779.1:c.832A=
|
XP_011532081.1:p.Thr278=
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|
XM_011533780.1:c.774-591A=
|
XP_011532082.1:n.774-591A=
|
|
XR_940447.1:n.900A=
|
|
|
NM_001355186.1:c.955A=
|
NP_001342115.1:p.Thr319=
|
|
NM_001365649.1:c.832A=
|
NP_001352578.1:p.Thr278=
|
|
NM_001365650.1:c.774-591A=
|
NP_001352579.1:n.774-591A=
|
|
NM_016006.5:c.955A=
|
NP_057090.2:p.Thr319=
|
|
NR_158560.1:n.966A=
|
|
|
NM_001355186.2:c.955A=
|
NP_001342115.1:p.Thr319=
|
|
NM_016006.6:c.955A=
MANE Select
|
NP_057090.2:p.Thr319=
|
|