ENST00000247933.9:c.1686G>C
|
ENSP00000247933.4:p.Gly562=
|
|
ENST00000514224.2:c.1686G>C
MANE Select
|
ENSP00000425081.2:p.Gly562=
|
|
ENST00000652070.1:n.1742G>C
|
|
|
ENST00000247933.8:c.1686G>C
|
ENSP00000247933.4:p.Gly562=
|
|
ENST00000514224.1:c.1290G>C
|
ENSP00000425081.1:p.Gly430=
|
|
ENST00000514417.1:n.78G>C
|
|
|
ENST00000514698.5:n.1793G>C
|
|
|
NM_000203.4:c.1686G>C
|
NP_000194.2:p.Gly562=
|
|
NR_110313.1:n.1774G>C
|
|
|
XM_006713882.2:c.1290G>C
|
XP_006713945.1:p.Gly430=
|
|
XM_011513459.1:c.1752G>C
|
XP_011511761.1:p.Gly584=
|
|
XM_011513460.1:c.1545G>C
|
XP_011511762.1:p.Gly515=
|
|
XM_011513461.1:c.1479G>C
|
XP_011511763.1:p.Gly493=
|
|
XM_011513462.1:c.1398G>C
|
XP_011511764.1:p.Gly466=
|
|
XM_011513463.1:c.1398G>C
|
XP_011511765.1:p.Gly466=
|
|
XR_924947.1:n.1942G>C
|
|
|
NM_000203.5:c.1686G>C
MANE Select
|
NP_000194.2:p.Gly562=
|
|
NM_001363576.1:c.1290G>C
|
NP_001350505.1:p.Gly430=
|
|
XM_011513461.2:c.1479G>C
|
XP_011511763.1:p.Gly493=
|
|
XM_017008163.1:c.726G>C
|
XP_016863652.1:p.Gly242=
|
|