ENST00000578493.2:n.747A>G
|
|
|
ENST00000699291.1:c.539A>G
|
ENSP00000514272.1:p.His180Arg
|
|
ENST00000699292.1:n.454A>G
|
|
|
ENST00000225275.4:c.1414A>G
MANE Select
|
ENSP00000225275.3:p.Met472Val
|
|
ENST00000225275.3:c.1414A>G
|
ENSP00000225275.3:p.Met472Val
|
|
NM_000250.1:c.1414A>G , LRG_84t1:c.1414A>G
|
NP_000241.1:p.Met472Val
|
|
XM_011524821.1:c.1600A>G
|
XP_011523123.1:p.Met534Val
|
|
XM_011524822.1:c.1129A>G
|
XP_011523124.1:p.Met377Val
|
|
XM_011524823.1:c.1439A>G
|
XP_011523125.1:p.His480Arg
|
|
NM_000250.2:c.1414A>G
MANE Select
|
NP_000241.1:p.Met472Val
|
|