|
NM_181458.4:c.994C>T
MANE Select
|
NP_852123.1:p.Gln332Ter
|
|
ENST00000392070.7:c.994C>T
MANE Select
|
ENSP00000375922.3:p.Gln332Ter
|
|
NM_001127366.2:c.991C>T
|
NP_001120838.1:p.Gln331Ter
|
|
NM_001127366.3:c.991C>T
|
NP_001120838.1:p.Gln331Ter
|
|
NM_181457.3:c.994C>T
|
NP_852122.1:p.Gln332Ter
|
|
NM_181457.4:c.994C>T
|
NP_852122.1:p.Gln332Ter
|
|
NM_181458.3:c.994C>T
|
NP_852123.1:p.Gln332Ter
|
|
NM_181459.3:c.994C>T
|
NP_852124.1:p.Gln332Ter
|
|
NM_181459.4:c.994C>T
|
NP_852124.1:p.Gln332Ter
|
|
NM_181460.3:c.994C>T
|
NP_852125.1:p.Gln332Ter
|
|
NM_181460.4:c.994C>T
|
NP_852125.1:p.Gln332Ter
|
|
NM_181461.3:c.994C>T
|
NP_852126.1:p.Gln332Ter
|
|
NM_181461.4:c.994C>T
|
NP_852126.1:p.Gln332Ter
|
|
ENST00000336840.10:c.994C>T
|
ENSP00000338767.5:p.Gln332Ter
|
|
ENST00000336840.11:c.994C>T
|
ENSP00000338767.5:p.Gln332Ter
|
|
ENST00000344493.8:c.994C>T
|
ENSP00000342092.4:p.Gln332Ter
|
|
ENST00000344493.9:c.994C>T
|
ENSP00000342092.4:p.Gln332Ter
|
|
ENST00000350526.8:c.994C>T
|
ENSP00000343052.4:p.Gln332Ter
|
|
ENST00000350526.9:c.994C>T
|
ENSP00000343052.4:p.Gln332Ter
|
|
ENST00000392069.6:c.994C>T
|
ENSP00000375921.2:p.Gln332Ter
|
|
ENST00000392070.6:c.994C>T
|
ENSP00000375922.2:p.Gln332Ter
|
|
ENST00000409551.7:c.991C>T
|
ENSP00000386750.3:p.Gln331Ter
|
|
ENST00000464706.5:n.418C>T
|
|
|
ENST00000464706.6:n.432C>T
|
|
|
ENST00000555548.1:n.225C>T
|
|
|
ENST00000644699.1:n.320C>T
|
|
|
ENST00000644937.1:n.266C>T
|
|
|
ENST00000646154.1:n.808C>T
|
|
|
XM_011511278.1:c.1138C>T
|
XP_011509580.1:p.Gln380Ter
|
|
XM_011511279.1:c.430C>T
|
XP_011509581.1:p.Gln144Ter
|
|
XR_001739903.1:n.240-77G>A
|
|