ENST00000369887.4:c.415G>T
MANE Select
|
ENSP00000358903.3:p.Asp139Tyr
|
|
ENST00000638190.1:c.415G>T
|
ENSP00000492539.1:p.Asp139Tyr
|
|
ENST00000638272.1:c.297+1790G>T
|
ENSP00000491508.1:n.297+1790G>T
|
|
ENST00000638971.1:c.415G>T
|
ENSP00000492313.1:p.Asp139Tyr
|
|
ENST00000639393.1:c.415G>T
|
ENSP00000492651.1:p.Asp139Tyr
|
|
ENST00000640633.1:n.177G>T
|
|
|
ENST00000369887.3:c.415G>T
|
ENSP00000358903.3:p.Asp139Tyr
|
|
ENST00000489268.1:n.669G>T
|
|
|
NM_000102.3:c.415G>T
|
NP_000093.1:p.Asp139Tyr
|
|
NM_000102.4:c.415G>T
MANE Select
|
NP_000093.1:p.Asp139Tyr
|
|