ENST00000578493.2:n.708T>C
|
|
|
ENST00000699291.1:c.500T>C
|
ENSP00000514272.1:p.Leu167Ser
|
|
ENST00000699292.1:n.415T>C
|
|
|
ENST00000225275.4:c.1375T>C
MANE Select
|
ENSP00000225275.3:p.Tyr459His
|
|
ENST00000225275.3:c.1375T>C
|
ENSP00000225275.3:p.Tyr459His
|
|
NM_000250.1:c.1375T>C , LRG_84t1:c.1375T>C
|
NP_000241.1:p.Tyr459His
|
|
XM_011524821.1:c.1561T>C
|
XP_011523123.1:p.Tyr521His
|
|
XM_011524822.1:c.1090T>C
|
XP_011523124.1:p.Tyr364His
|
|
XM_011524823.1:c.1400T>C
|
XP_011523125.1:p.Leu467Ser
|
|
NM_000250.2:c.1375T>C
MANE Select
|
NP_000241.1:p.Tyr459His
|
|