ENST00000624552.4:c.14927G>C
|
ENSP00000485357.2:p.Arg4976Pro
|
|
ENST00000683500.2:c.14984G>C
MANE Select
|
ENSP00000508292.2:p.Arg4995Pro
|
|
ENST00000623487.1:n.3330G>C
|
|
|
ENST00000624552.3:c.14924G>C
|
ENSP00000485357.1:p.Arg4975Pro
|
|
NM_001291815.1:c.14984G>C
|
NP_001278744.1:p.Arg4995Pro
|
|
XM_011518465.1:c.14861G>C
|
XP_011516767.1:p.Arg4954Pro
|
|
XM_011518466.1:c.14852G>C
|
XP_011516768.1:p.Arg4951Pro
|
|
XM_011518467.1:c.14807G>C
|
XP_011516769.1:p.Arg4936Pro
|
|
NM_001291815.2:c.14984G>C
MANE Select
|
NP_001278744.1:p.Arg4995Pro
|
|
XM_011518465.2:c.14861G>C
|
XP_011516767.1:p.Arg4954Pro
|
|
XM_011518466.2:c.14852G>C
|
XP_011516768.1:p.Arg4951Pro
|
|
XM_011518467.2:c.14807G>C
|
XP_011516769.1:p.Arg4936Pro
|
|
XM_017014585.1:c.11765G>C
|
XP_016870074.1:p.Arg3922Pro
|
|
XM_017014586.1:c.7562G>C
|
XP_016870075.1:p.Arg2521Pro
|
|
XR_001746957.1:n.92+184C>G
|
|
|
XR_001746958.1:n.92+184C>G
|
|
|