ENST00000336411.7:c.1375G>T
|
ENSP00000337915.3:p.Asp459Tyr
|
|
ENST00000651162.1:n.717G>T
|
|
|
ENST00000651514.1:c.1282G>T
MANE Select
|
ENSP00000498939.1:p.Asp428Tyr
|
|
ENST00000651783.1:c.823G>T
|
ENSP00000498924.1:p.Asp275Tyr
|
|
ENST00000652018.1:c.1135G>T
|
ENSP00000498733.1:p.Asp379Tyr
|
|
ENST00000336411.6:c.1282G>T
|
ENSP00000337915.2:p.Asp428Tyr
|
|
ENST00000354593.6:c.832G>T
|
ENSP00000346607.2:p.Asp278Tyr
|
|
NM_001202855.2:c.1279G>T
|
NP_001189784.1:p.Asp427Tyr
|
|
NM_017460.5:c.1282G>T
|
NP_059488.2:p.Asp428Tyr
|
|
XM_011515841.1:c.1375G>T
|
XP_011514143.1:p.Asp459Tyr
|
|
XM_011515842.1:c.1372G>T
|
XP_011514144.1:p.Asp458Tyr
|
|
NM_017460.6:c.1282G>T
MANE Select
|
NP_059488.2:p.Asp428Tyr
|
|
NM_001202855.3:c.1279G>T
|
NP_001189784.1:p.Asp427Tyr
|
|