ENST00000262367.10:c.4086G>C
MANE Select
|
ENSP00000262367.5:p.Val1362=
|
|
ENST00000262367.9:c.4086G>C
|
ENSP00000262367.5:p.Val1362=
|
|
ENST00000382070.7:c.3972G>C
|
ENSP00000371502.3:p.Val1324=
|
|
ENST00000570939.2:c.2721G>C
|
ENSP00000461002.2:p.Val907=
|
|
ENST00000572569.1:n.550G>C
|
|
|
ENST00000573517.6:c.392G>C
|
|
|
ENST00000574740.1:n.168G>C
|
|
|
ENST00000576720.1:n.3023G>C
|
|
|
NM_001079846.1:c.3972G>C
|
NP_001073315.1:p.Val1324=
|
|
NM_004380.2:c.4086G>C
|
NP_004371.2:p.Val1362=
|
|
XM_005255124.3:c.4041G>C
|
XP_005255181.1:p.Val1347=
|
|
XM_005255125.3:c.3669G>C
|
XP_005255182.1:p.Val1223=
|
|
XM_006720848.2:c.4086G>C
|
XP_006720911.1:p.Val1362=
|
|
XM_011522380.1:c.4032G>C
|
XP_011520682.1:p.Val1344=
|
|
XM_011522381.1:c.3333G>C
|
XP_011520683.1:p.Val1111=
|
|
XM_005255124.4:c.4041G>C
|
XP_005255181.1:p.Val1347=
|
|
XM_005255125.4:c.3669G>C
|
XP_005255182.1:p.Val1223=
|
|
XM_006720848.3:c.4086G>C
|
XP_006720911.1:p.Val1362=
|
|
XM_011522381.2:c.3333G>C
|
XP_011520683.1:p.Val1111=
|
|
XM_017022944.1:c.4080G>C
|
XP_016878433.1:p.Val1360=
|
|
NM_004380.3:c.4086G>C
MANE Select
|
NP_004371.2:p.Val1362=
|
|