ENST00000370263.9:c.546G>A
MANE Select
|
ENSP00000359285.4:p.Trp182Ter
|
|
ENST00000370263.8:c.546G>A
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ENSP00000359285.4:p.Trp182Ter
|
|
ENST00000463705.5:n.1194G>A
|
|
|
ENST00000467563.3:n.616G>A
|
|
|
ENST00000498043.6:c.570G>A
|
|
|
ENST00000615287.4:c.333G>A
|
ENSP00000483388.1:p.Trp111Ter
|
|
ENST00000627000.1:c.*235G>A
|
ENSP00000486914.1:n.*235G>A
|
|
ENST00000630240.1:n.267G>A
|
|
|
NM_000744.6:c.546G>A
|
NP_000735.1:p.Trp182Ter
|
|
NM_001256573.1:c.18G>A
|
NP_001243502.1:p.Trp6Ter
|
|
NR_046317.1:n.802G>A
|
|
|
XM_011528524.1:c.333G>A
|
XP_011526826.1:p.Trp111Ter
|
|
XM_017027625.2:c.18G>A
|
XP_016883114.1:p.Trp6Ter
|
|
XM_024451822.1:c.18G>A
|
XP_024307590.1:p.Trp6Ter
|
|
NM_001256573.2:c.18G>A
|
NP_001243502.1:p.Trp6Ter
|
|
NR_046317.2:n.755G>A
|
|
|
NM_000744.7:c.546G>A
MANE Select
|
NP_000735.1:p.Trp182Ter
|
|