ENST00000336411.7:c.1419C>T
|
ENSP00000337915.3:p.Cys473=
|
|
ENST00000651162.1:n.761C>T
|
|
|
ENST00000651514.1:c.1326C>T
MANE Select
|
ENSP00000498939.1:p.Cys442=
|
|
ENST00000651783.1:c.867C>T
|
ENSP00000498924.1:p.Cys289=
|
|
ENST00000652018.1:c.1179C>T
|
ENSP00000498733.1:p.Cys393=
|
|
ENST00000336411.6:c.1326C>T
|
ENSP00000337915.2:p.Cys442=
|
|
ENST00000354593.6:c.876C>T
|
ENSP00000346607.2:p.Cys292=
|
|
NM_001202855.2:c.1323C>T
|
NP_001189784.1:p.Cys441=
|
|
NM_017460.5:c.1326C>T
|
NP_059488.2:p.Cys442=
|
|
XM_011515841.1:c.1419C>T
|
XP_011514143.1:p.Cys473=
|
|
XM_011515842.1:c.1416C>T
|
XP_011514144.1:p.Cys472=
|
|
NM_017460.6:c.1326C>T
MANE Select
|
NP_059488.2:p.Cys442=
|
|
NM_001202855.3:c.1323C>T
|
NP_001189784.1:p.Cys441=
|
|