ENST00000247933.9:c.814A>G
|
ENSP00000247933.4:p.Ile272Val
|
|
ENST00000514224.2:c.814A>G
MANE Select
|
ENSP00000425081.2:p.Ile272Val
|
|
ENST00000652070.1:n.870A>G
|
|
|
ENST00000247933.8:c.814A>G
|
ENSP00000247933.4:p.Ile272Val
|
|
ENST00000502910.5:c.673A>G
|
|
|
ENST00000514192.5:c.631A>G
|
ENSP00000423685.1:p.Ile211Val
|
|
ENST00000514224.1:c.418A>G
|
ENSP00000425081.1:p.Ile140Val
|
|
ENST00000514698.5:n.814A>G
|
|
|
NM_000203.4:c.814A>G
|
NP_000194.2:p.Ile272Val
|
|
NR_110313.1:n.902A>G
|
|
|
XM_006713882.2:c.418A>G
|
XP_006713945.1:p.Ile140Val
|
|
XM_011513459.1:c.773A>G
|
XP_011511761.1:p.His258Arg
|
|
XM_011513460.1:c.673A>G
|
XP_011511762.1:p.Ile225Val
|
|
XM_011513461.1:c.607A>G
|
XP_011511763.1:p.Ile203Val
|
|
XM_011513462.1:c.526A>G
|
XP_011511764.1:p.Ile176Val
|
|
XM_011513463.1:c.526A>G
|
XP_011511765.1:p.Ile176Val
|
|
XR_924947.1:n.883A>G
|
|
|
NM_000203.5:c.814A>G
MANE Select
|
NP_000194.2:p.Ile272Val
|
|
NM_001363576.1:c.418A>G
|
NP_001350505.1:p.Ile140Val
|
|
XM_011513461.2:c.607A>G
|
XP_011511763.1:p.Ile203Val
|
|
XM_017008163.1:c.-147A>G
|
XP_016863652.1:n.-147A>G
|
|