ENST00000268695.10:c.758+117C>T
MANE Select
|
ENSP00000268695.5:n.758+117C>T
|
|
ENST00000268695.9:c.758+117C>T
|
ENSP00000268695.5:n.758+117C>T
|
|
ENST00000562593.5:n.4167+117C>T
|
|
|
ENST00000562931.5:n.346+117C>T
|
|
|
ENST00000567525.5:c.439+117C>T
|
ENSP00000454484.1:n.439+117C>T
|
|
ENST00000568613.5:c.877+117C>T
|
ENSP00000457921.1:n.877+117C>T
|
|
NM_000512.4:c.758+117C>T
|
NP_000503.1:n.758+117C>T
|
|
XM_005256301.2:c.758+117C>T
|
XP_005256358.1:n.758+117C>T
|
|
XM_005256302.1:c.776+117C>T
|
XP_005256359.1:n.776+117C>T
|
|
XM_011522982.1:c.776+117C>T
|
XP_011521284.1:n.776+117C>T
|
|
XM_011522984.1:c.776+117C>T
|
XP_011521286.1:n.776+117C>T
|
|
NM_001323543.1:c.203+117C>T
|
NP_001310472.1:n.203+117C>T
|
|
NM_001323544.1:c.776+117C>T
|
NP_001310473.1:n.776+117C>T
|
|
XM_005256301.3:c.758+117C>T
|
XP_005256358.1:n.758+117C>T
|
|
XM_011522982.2:c.776+117C>T
|
XP_011521284.1:n.776+117C>T
|
|
XM_017023111.2:c.776+117C>T
|
XP_016878600.1:n.776+117C>T
|
|
XM_017023112.2:c.776+117C>T
|
XP_016878601.1:n.776+117C>T
|
|
XM_017023113.1:c.203+117C>T
|
XP_016878602.1:n.203+117C>T
|
|
NM_000512.5:c.758+117C>T
MANE Select
|
NP_000503.1:n.758+117C>T
|
|
NM_001323543.2:c.203+117C>T
|
NP_001310472.1:n.203+117C>T
|
|
NM_001323544.2:c.776+117C>T
|
NP_001310473.1:n.776+117C>T
|
|