ENST00000578493.2:n.756T>C
|
|
|
ENST00000699291.1:c.548T>C
|
ENSP00000514272.1:p.Val183Ala
|
|
ENST00000699292.1:n.463T>C
|
|
|
ENST00000225275.4:c.1423T>C
MANE Select
|
ENSP00000225275.3:p.Tyr475His
|
|
ENST00000225275.3:c.1423T>C
|
ENSP00000225275.3:p.Tyr475His
|
|
NM_000250.1:c.1423T>C , LRG_84t1:c.1423T>C
|
NP_000241.1:p.Tyr475His
|
|
XM_011524821.1:c.1609T>C
|
XP_011523123.1:p.Tyr537His
|
|
XM_011524822.1:c.1138T>C
|
XP_011523124.1:p.Tyr380His
|
|
XM_011524823.1:c.1448T>C
|
XP_011523125.1:p.Val483Ala
|
|
NM_000250.2:c.1423T>C
MANE Select
|
NP_000241.1:p.Tyr475His
|
|