ENST00000357578.8:c.536T>C
MANE Select
|
ENSP00000350191.3:p.Ile179Thr
|
|
ENST00000672352.1:c.299T>C
|
ENSP00000500876.1:p.Ile100Thr
|
|
ENST00000672557.1:c.454T>C
|
|
|
ENST00000672652.1:c.457T>C
|
|
|
ENST00000675422.1:n.1296T>C
|
|
|
ENST00000348925.2:c.536T>C
|
ENSP00000314649.3:p.Ile179Thr
|
|
ENST00000357578.7:c.536T>C
|
ENSP00000350191.3:p.Ile179Thr
|
|
ENST00000491546.5:c.452T>C
|
ENSP00000417687.1:p.Ile151Thr
|
|
NM_001080.3:c.536T>C
MANE Select
|
NP_001071.1:p.Ile179Thr
|
|
NM_170740.1:c.536T>C
|
NP_733936.1:p.Ile179Thr
|
|
NM_001368954.1:c.536T>C
|
NP_001355883.1:p.Ile179Thr
|
|