ENST00000247933.9:c.1136T>C
|
ENSP00000247933.4:p.Val379Ala
|
|
ENST00000514224.2:c.1136T>C
MANE Select
|
ENSP00000425081.2:p.Val379Ala
|
|
ENST00000652070.1:n.1192T>C
|
|
|
ENST00000247933.8:c.1136T>C
|
ENSP00000247933.4:p.Val379Ala
|
|
ENST00000514224.1:c.740T>C
|
ENSP00000425081.1:p.Val247Ala
|
|
ENST00000514698.5:n.1243T>C
|
|
|
NM_000203.4:c.1136T>C
|
NP_000194.2:p.Val379Ala
|
|
NR_110313.1:n.1224T>C
|
|
|
XM_006713882.2:c.740T>C
|
XP_006713945.1:p.Val247Ala
|
|
XM_011513459.1:c.1202T>C
|
XP_011511761.1:p.Val401Ala
|
|
XM_011513460.1:c.995T>C
|
XP_011511762.1:p.Val332Ala
|
|
XM_011513461.1:c.929T>C
|
XP_011511763.1:p.Val310Ala
|
|
XM_011513462.1:c.848T>C
|
XP_011511764.1:p.Val283Ala
|
|
XM_011513463.1:c.848T>C
|
XP_011511765.1:p.Val283Ala
|
|
XR_924947.1:n.1205T>C
|
|
|
NM_000203.5:c.1136T>C
MANE Select
|
NP_000194.2:p.Val379Ala
|
|
NM_001363576.1:c.740T>C
|
NP_001350505.1:p.Val247Ala
|
|
XM_011513461.2:c.929T>C
|
XP_011511763.1:p.Val310Ala
|
|
XM_017008163.1:c.176T>C
|
XP_016863652.1:p.Val59Ala
|
|