ENST00000624552.4:c.14948G>C
|
ENSP00000485357.2:p.Arg4983Pro
|
|
ENST00000683500.2:c.15005G>C
MANE Select
|
ENSP00000508292.2:p.Arg5002Pro
|
|
ENST00000623487.1:n.3351G>C
|
|
|
ENST00000624552.3:c.14945G>C
|
ENSP00000485357.1:p.Arg4982Pro
|
|
NM_001291815.1:c.15005G>C
|
NP_001278744.1:p.Arg5002Pro
|
|
XM_011518465.1:c.14882G>C
|
XP_011516767.1:p.Arg4961Pro
|
|
XM_011518466.1:c.14873G>C
|
XP_011516768.1:p.Arg4958Pro
|
|
XM_011518467.1:c.14828G>C
|
XP_011516769.1:p.Arg4943Pro
|
|
NM_001291815.2:c.15005G>C
MANE Select
|
NP_001278744.1:p.Arg5002Pro
|
|
XM_011518465.2:c.14882G>C
|
XP_011516767.1:p.Arg4961Pro
|
|
XM_011518466.2:c.14873G>C
|
XP_011516768.1:p.Arg4958Pro
|
|
XM_011518467.2:c.14828G>C
|
XP_011516769.1:p.Arg4943Pro
|
|
XM_017014585.1:c.11786G>C
|
XP_016870074.1:p.Arg3929Pro
|
|
XM_017014586.1:c.7583G>C
|
XP_016870075.1:p.Arg2528Pro
|
|
XR_001746957.1:n.92+163C>G
|
|
|
XR_001746958.1:n.92+163C>G
|
|
|