ENST00000624552.4:c.14938G>C
|
ENSP00000485357.2:p.Asp4980His
|
|
ENST00000683500.2:c.14995G>C
MANE Select
|
ENSP00000508292.2:p.Asp4999His
|
|
ENST00000623487.1:n.3341G>C
|
|
|
ENST00000624552.3:c.14935G>C
|
ENSP00000485357.1:p.Asp4979His
|
|
NM_001291815.1:c.14995G>C
|
NP_001278744.1:p.Asp4999His
|
|
XM_011518465.1:c.14872G>C
|
XP_011516767.1:p.Asp4958His
|
|
XM_011518466.1:c.14863G>C
|
XP_011516768.1:p.Asp4955His
|
|
XM_011518467.1:c.14818G>C
|
XP_011516769.1:p.Asp4940His
|
|
NM_001291815.2:c.14995G>C
MANE Select
|
NP_001278744.1:p.Asp4999His
|
|
XM_011518465.2:c.14872G>C
|
XP_011516767.1:p.Asp4958His
|
|
XM_011518466.2:c.14863G>C
|
XP_011516768.1:p.Asp4955His
|
|
XM_011518467.2:c.14818G>C
|
XP_011516769.1:p.Asp4940His
|
|
XM_017014585.1:c.11776G>C
|
XP_016870074.1:p.Asp3926His
|
|
XM_017014586.1:c.7573G>C
|
XP_016870075.1:p.Asp2525His
|
|
XR_001746957.1:n.92+173C>G
|
|
|
XR_001746958.1:n.92+173C>G
|
|
|