ENST00000624552.4:c.14964C>G
|
ENSP00000485357.2:p.Ser4988=
|
|
ENST00000683500.2:c.15021C>G
MANE Select
|
ENSP00000508292.2:p.Ser5007=
|
|
ENST00000623487.1:n.3367C>G
|
|
|
ENST00000624552.3:c.14961C>G
|
ENSP00000485357.1:p.Ser4987=
|
|
NM_001291815.1:c.15021C>G
|
NP_001278744.1:p.Ser5007=
|
|
XM_011518465.1:c.14898C>G
|
XP_011516767.1:p.Ser4966=
|
|
XM_011518466.1:c.14889C>G
|
XP_011516768.1:p.Ser4963=
|
|
XM_011518467.1:c.14844C>G
|
XP_011516769.1:p.Ser4948=
|
|
NM_001291815.2:c.15021C>G
MANE Select
|
NP_001278744.1:p.Ser5007=
|
|
XM_011518465.2:c.14898C>G
|
XP_011516767.1:p.Ser4966=
|
|
XM_011518466.2:c.14889C>G
|
XP_011516768.1:p.Ser4963=
|
|
XM_011518467.2:c.14844C>G
|
XP_011516769.1:p.Ser4948=
|
|
XM_017014585.1:c.11802C>G
|
XP_016870074.1:p.Ser3934=
|
|
XM_017014586.1:c.7599C>G
|
XP_016870075.1:p.Ser2533=
|
|
XR_001746957.1:n.92+147G>C
|
|
|
XR_001746958.1:n.92+147G>C
|
|
|