ENST00000578493.2:n.814T>C
|
|
|
ENST00000699291.1:c.606T>C
|
ENSP00000514272.1:n.606T>C
|
|
ENST00000699292.1:n.521T>C
|
|
|
ENST00000225275.4:c.1481T>C
MANE Select
|
ENSP00000225275.3:p.Phe494Ser
|
|
ENST00000225275.3:c.1481T>C
|
ENSP00000225275.3:p.Phe494Ser
|
|
NM_000250.1:c.1481T>C , LRG_84t1:c.1481T>C
|
NP_000241.1:p.Phe494Ser
|
|
XM_011524821.1:c.1667T>C
|
XP_011523123.1:p.Phe556Ser
|
|
XM_011524822.1:c.1196T>C
|
XP_011523124.1:p.Phe399Ser
|
|
XM_011524823.1:c.*30T>C
|
XP_011523125.1:n.*30T>C
|
|
NM_000250.2:c.1481T>C
MANE Select
|
NP_000241.1:p.Phe494Ser
|
|