ENST00000247933.9:c.1254G>C
|
ENSP00000247933.4:p.Val418=
|
|
ENST00000514224.2:c.1254G>C
MANE Select
|
ENSP00000425081.2:p.Val418=
|
|
ENST00000652070.1:n.1310G>C
|
|
|
ENST00000247933.8:c.1254G>C
|
ENSP00000247933.4:p.Val418=
|
|
ENST00000502829.1:n.56G>C
|
|
|
ENST00000514224.1:c.858G>C
|
ENSP00000425081.1:p.Val286=
|
|
ENST00000514698.5:n.1361G>C
|
|
|
NM_000203.4:c.1254G>C
|
NP_000194.2:p.Val418=
|
|
NR_110313.1:n.1342G>C
|
|
|
XM_006713882.2:c.858G>C
|
XP_006713945.1:p.Val286=
|
|
XM_011513459.1:c.1320G>C
|
XP_011511761.1:p.Val440=
|
|
XM_011513460.1:c.1113G>C
|
XP_011511762.1:p.Val371=
|
|
XM_011513461.1:c.1047G>C
|
XP_011511763.1:p.Val349=
|
|
XM_011513462.1:c.966G>C
|
XP_011511764.1:p.Val322=
|
|
XM_011513463.1:c.966G>C
|
XP_011511765.1:p.Val322=
|
|
XR_924947.1:n.1323G>C
|
|
|
NM_000203.5:c.1254G>C
MANE Select
|
NP_000194.2:p.Val418=
|
|
NM_001363576.1:c.858G>C
|
NP_001350505.1:p.Val286=
|
|
XM_011513461.2:c.1047G>C
|
XP_011511763.1:p.Val349=
|
|
XM_017008163.1:c.294G>C
|
XP_016863652.1:p.Val98=
|
|