ENST00000578493.2:n.825T>C
|
|
|
ENST00000699291.1:c.617T>C
|
ENSP00000514272.1:n.617T>C
|
|
ENST00000699292.1:n.532T>C
|
|
|
ENST00000225275.4:c.1492T>C
MANE Select
|
ENSP00000225275.3:p.Phe498Leu
|
|
ENST00000225275.3:c.1492T>C
|
ENSP00000225275.3:p.Phe498Leu
|
|
NM_000250.1:c.1492T>C , LRG_84t1:c.1492T>C
|
NP_000241.1:p.Phe498Leu
|
|
XM_011524821.1:c.1678T>C
|
XP_011523123.1:p.Phe560Leu
|
|
XM_011524822.1:c.1207T>C
|
XP_011523124.1:p.Phe403Leu
|
|
XM_011524823.1:c.*41T>C
|
XP_011523125.1:n.*41T>C
|
|
NM_000250.2:c.1492T>C
MANE Select
|
NP_000241.1:p.Phe498Leu
|
|