ENST00000578493.2:n.779C>T
|
|
|
ENST00000699291.1:c.571C>T
|
ENSP00000514272.1:p.Gln191Ter
|
|
ENST00000699292.1:n.486C>T
|
|
|
ENST00000225275.4:c.1446C>T
MANE Select
|
ENSP00000225275.3:p.Tyr482=
|
|
ENST00000225275.3:c.1446C>T
|
ENSP00000225275.3:p.Tyr482=
|
|
NM_000250.1:c.1446C>T , LRG_84t1:c.1446C>T
|
NP_000241.1:p.Tyr482=
|
|
XM_011524821.1:c.1632C>T
|
XP_011523123.1:p.Tyr544=
|
|
XM_011524822.1:c.1161C>T
|
XP_011523124.1:p.Tyr387=
|
|
XM_011524823.1:c.1471C>T
|
XP_011523125.1:p.Gln491Ter
|
|
NM_000250.2:c.1446C>T
MANE Select
|
NP_000241.1:p.Tyr482=
|
|