ENST00000292408.9:c.1307T>C
MANE Select
|
ENSP00000292408.4:p.Val436Ala
|
|
ENST00000292408.8:c.1307T>C
|
ENSP00000292408.4:p.Val436Ala
|
|
ENST00000393637.5:c.1187T>C
|
ENSP00000377254.1:p.Val396Ala
|
|
ENST00000393648.6:c.1153T>C
|
ENSP00000377259.2:p.Cys385Arg
|
|
ENST00000502906.5:c.1307T>C
|
ENSP00000424960.1:p.Val436Ala
|
|
ENST00000508139.1:n.685T>C
|
|
|
ENST00000511076.1:c.201T>C
|
|
|
NM_001291980.1:c.1153T>C
|
NP_001278909.1:p.Cys385Arg
|
|
NM_002011.4:c.1307T>C
|
NP_002002.3:p.Val436Ala
|
|
NM_022963.3:c.1187T>C
|
NP_075252.2:p.Val396Ala
|
|
NM_213647.2:c.1307T>C
|
NP_998812.1:p.Val436Ala
|
|
XM_005265838.2:c.1307T>C
|
XP_005265895.1:p.Val436Ala
|
|
XM_011534464.1:c.1400T>C
|
XP_011532766.1:p.Val467Ala
|
|
XM_011534465.1:c.989T>C
|
XP_011532767.1:p.Val330Ala
|
|
XR_941090.1:n.1352T>C
|
|
|
NM_001354984.1:c.1307T>C
|
NP_001341913.1:p.Val436Ala
|
|
NM_213647.3:c.1307T>C
MANE Select
|
NP_998812.1:p.Val436Ala
|
|
NM_001291980.2:c.1153T>C
|
NP_001278909.1:p.Cys385Arg
|
|
NM_001354984.2:c.1307T>C
|
NP_001341913.1:p.Val436Ala
|
|
NM_002011.5:c.1307T>C
|
NP_002002.3:p.Val436Ala
|
|