ENST00000609686.4:c.1543A>G
MANE Select
|
ENSP00000477455.1:p.Ile515Val
|
|
ENST00000609686.3:c.1543A>G
|
ENSP00000477455.1:p.Ile515Val
|
|
NM_000834.3:c.1543A>G
|
NP_000825.2:p.Ile515Val
|
|
XM_011520628.1:c.1543A>G
|
XP_011518930.1:p.Ile515Val
|
|
XM_011520629.1:c.1543A>G
|
XP_011518931.1:p.Ile515Val
|
|
XM_011520630.1:c.1543A>G
|
XP_011518932.1:p.Ile515Val
|
|
XR_931372.1:n.306T>C
|
|
|
XR_931373.1:n.446T>C
|
|
|
XR_931374.1:n.245T>C
|
|
|
NM_000834.4:c.1543A>G
|
NP_000825.2:p.Ile515Val
|
|
XM_011520628.2:c.1543A>G
|
XP_011518930.1:p.Ile515Val
|
|
XM_011520629.2:c.1543A>G
|
XP_011518931.1:p.Ile515Val
|
|
XM_017019219.2:c.1543A>G
|
XP_016874708.1:p.Ile515Val
|
|
XR_001749013.1:n.727T>C
|
|
|
XR_931372.2:n.443T>C
|
|
|
XR_931373.2:n.585T>C
|
|
|
NM_000834.5:c.1543A>G
MANE Select
|
NP_000825.2:p.Ile515Val
|
|