ENST00000247933.9:c.1700T>G
|
ENSP00000247933.4:p.Val567Gly
|
|
ENST00000514224.2:c.1700T>G
MANE Select
|
ENSP00000425081.2:p.Val567Gly
|
|
ENST00000652070.1:n.1756T>G
|
|
|
ENST00000247933.8:c.1700T>G
|
ENSP00000247933.4:p.Val567Gly
|
|
ENST00000514224.1:c.1304T>G
|
ENSP00000425081.1:p.Val435Gly
|
|
ENST00000514417.1:n.92T>G
|
|
|
ENST00000514698.5:n.1807T>G
|
|
|
NM_000203.4:c.1700T>G
|
NP_000194.2:p.Val567Gly
|
|
NR_110313.1:n.1788T>G
|
|
|
XM_006713882.2:c.1304T>G
|
XP_006713945.1:p.Val435Gly
|
|
XM_011513459.1:c.1766T>G
|
XP_011511761.1:p.Val589Gly
|
|
XM_011513460.1:c.1559T>G
|
XP_011511762.1:p.Val520Gly
|
|
XM_011513461.1:c.1493T>G
|
XP_011511763.1:p.Val498Gly
|
|
XM_011513462.1:c.1412T>G
|
XP_011511764.1:p.Val471Gly
|
|
XM_011513463.1:c.1412T>G
|
XP_011511765.1:p.Val471Gly
|
|
XR_924947.1:n.1956T>G
|
|
|
NM_000203.5:c.1700T>G
MANE Select
|
NP_000194.2:p.Val567Gly
|
|
NM_001363576.1:c.1304T>G
|
NP_001350505.1:p.Val435Gly
|
|
XM_011513461.2:c.1493T>G
|
XP_011511763.1:p.Val498Gly
|
|
XM_017008163.1:c.740T>G
|
XP_016863652.1:p.Val247Gly
|
|