ENST00000624552.4:c.14900G>A
|
ENSP00000485357.2:p.Arg4967Gln
|
|
ENST00000683500.2:c.14957G>A
MANE Select
|
ENSP00000508292.2:p.Arg4986Gln
|
|
ENST00000623487.1:n.3303G>A
|
|
|
ENST00000624552.3:c.14897G>A
|
ENSP00000485357.1:p.Arg4966Gln
|
|
NM_001291815.1:c.14957G>A
|
NP_001278744.1:p.Arg4986Gln
|
|
XM_011518465.1:c.14834G>A
|
XP_011516767.1:p.Arg4945Gln
|
|
XM_011518466.1:c.14825G>A
|
XP_011516768.1:p.Arg4942Gln
|
|
XM_011518467.1:c.14780G>A
|
XP_011516769.1:p.Arg4927Gln
|
|
NM_001291815.2:c.14957G>A
MANE Select
|
NP_001278744.1:p.Arg4986Gln
|
|
XM_011518465.2:c.14834G>A
|
XP_011516767.1:p.Arg4945Gln
|
|
XM_011518466.2:c.14825G>A
|
XP_011516768.1:p.Arg4942Gln
|
|
XM_011518467.2:c.14780G>A
|
XP_011516769.1:p.Arg4927Gln
|
|
XM_017014585.1:c.11738G>A
|
XP_016870074.1:p.Arg3913Gln
|
|
XM_017014586.1:c.7535G>A
|
XP_016870075.1:p.Arg2512Gln
|
|
XR_001746957.1:n.92+211C>T
|
|
|
XR_001746958.1:n.92+211C>T
|
|
|