ENST00000474370.2:n.2397T>G
|
|
|
ENST00000492391.2:n.1548T>G
|
|
|
ENST00000682645.1:n.3495T>G
|
|
|
ENST00000683432.1:c.*599T>G
|
ENSP00000508174.1:n.*599T>G
|
|
ENST00000684207.1:c.424T>G
|
ENSP00000506942.1:p.Tyr142Asp
|
|
ENST00000297157.8:c.424T>G
MANE Select
|
ENSP00000297157.3:p.Tyr142Asp
|
|
ENST00000297157.7:c.424T>G
|
ENSP00000297157.3:p.Tyr142Asp
|
|
ENST00000448915.1:c.322T>G
|
ENSP00000411577.1:p.Tyr108Asp
|
|
NM_203288.1:c.424T>G
|
NP_976033.1:p.Tyr142Asp
|
|
XM_011515468.1:c.322T>G
|
XP_011513770.1:p.Tyr108Asp
|
|
XM_011515468.3:c.322T>G
|
XP_011513770.1:p.Tyr108Asp
|
|
NM_203288.2:c.424T>G
MANE Select
|
NP_976033.1:p.Tyr142Asp
|
|