ENST00000262418.12:c.1961G>T
MANE Select
|
ENSP00000262418.6:p.Gly654Val
|
|
ENST00000262418.10:c.1961G>T
|
ENSP00000262418.6:p.Gly654Val
|
|
ENST00000399246.3:c.863G>T
|
ENSP00000382190.3:p.Gly288Val
|
|
NM_000342.3:c.1961G>T
|
NP_000333.1:p.Gly654Val
|
|
XM_005257593.3:c.1766G>T
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XP_005257650.1:p.Gly589Val
|
|
XM_011525129.1:c.1871G>T
|
XP_011523431.1:p.Gly624Val
|
|
XM_011525130.1:c.1961G>T
|
XP_011523432.1:p.Gly654Val
|
|
XM_011525131.1:c.1961G>T
|
XP_011523433.1:p.Gly654Val
|
|
XM_005257593.5:c.1766G>T
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XP_005257650.1:p.Gly589Val
|
|
XM_011525129.2:c.1871G>T
|
XP_011523431.1:p.Gly624Val
|
|
NM_000342.4:c.1961G>T
MANE Select
|
NP_000333.1:p.Gly654Val
|
|