ENST00000624552.4:c.14838G>T
|
ENSP00000485357.2:p.Gly4946=
|
|
ENST00000683500.2:c.14895G>T
MANE Select
|
ENSP00000508292.2:p.Gly4965=
|
|
ENST00000623487.1:n.3241G>T
|
|
|
ENST00000624552.3:c.14835G>T
|
ENSP00000485357.1:p.Gly4945=
|
|
NM_001291815.1:c.14895G>T
|
NP_001278744.1:p.Gly4965=
|
|
XM_011518465.1:c.14772G>T
|
XP_011516767.1:p.Gly4924=
|
|
XM_011518466.1:c.14763G>T
|
XP_011516768.1:p.Gly4921=
|
|
XM_011518467.1:c.14718G>T
|
XP_011516769.1:p.Gly4906=
|
|
NM_001291815.2:c.14895G>T
MANE Select
|
NP_001278744.1:p.Gly4965=
|
|
XM_011518465.2:c.14772G>T
|
XP_011516767.1:p.Gly4924=
|
|
XM_011518466.2:c.14763G>T
|
XP_011516768.1:p.Gly4921=
|
|
XM_011518467.2:c.14718G>T
|
XP_011516769.1:p.Gly4906=
|
|
XM_017014585.1:c.11676G>T
|
XP_016870074.1:p.Gly3892=
|
|
XM_017014586.1:c.7473G>T
|
XP_016870075.1:p.Gly2491=
|
|
XR_001746957.1:n.92+273C>A
|
|
|
XR_001746958.1:n.92+273C>A
|
|
|