NM_001831.4:c.1191C>T
MANE Select
|
NP_001822.3:p.Asp397=
|
ENST00000316403.15:c.1191C>T
MANE Select
|
ENSP00000315130.10:p.Asp397=
|
NM_001831.3:c.1191C>T
|
NP_001822.3:p.Asp397=
|
NR_038335.1:n.1512C>T
|
|
NR_038335.2:n.1446C>T
|
|
NR_045494.1:n.1371C>T
|
|
ENST00000316403.14:c.1191C>T
|
ENSP00000315130.10:p.Asp397=
|
ENST00000405140.7:c.1191C>T
|
ENSP00000385419.3:p.Asp397=
|
ENST00000521770.1:c.263C>T
|
|
ENST00000522098.1:c.778C>T
|
|
ENST00000522299.5:n.2403C>T
|
|
ENST00000523500.5:c.1191C>T
|
ENSP00000429620.1:p.Asp397=
|
XM_006716284.1:c.1347C>T
|
XP_006716347.1:p.Asp449=
|
XM_006716284.3:c.1347C>T
|
XP_006716347.1:p.Asp449=
|