|
ENST00000300591.11:c.524G>T
|
ENSP00000300591.6:p.Gly175Val
|
|
|
ENST00000579038.6:c.236G>T
|
ENSP00000463285.1:p.Gly79Val
|
|
|
ENST00000582408.6:c.524G>T
|
ENSP00000461964.1:p.Gly175Val
|
|
|
ENST00000642948.1:c.3857G>T
MANE Select
|
ENSP00000496347.1:p.Gly1286Val
|
|
|
ENST00000300591.10:c.524G>T
|
ENSP00000300591.6:p.Gly175Val
|
|
|
ENST00000335730.6:n.3170G>T
|
|
|
|
ENST00000441551.6:c.3239G>T
|
ENSP00000387621.2:p.Gly1080Val
|
|
|
ENST00000536111.1:c.563G>T
|
ENSP00000440060.1:p.Gly188Val
|
|
|
ENST00000536736.5:c.3857G>T
|
ENSP00000444586.1:p.Gly1286Val
|
|
|
ENST00000579038.5:c.236G>T
|
ENSP00000463285.1:p.Gly79Val
|
|
|
ENST00000582408.5:c.524G>T
|
ENSP00000461964.1:p.Gly175Val
|
|
|
NM_001145472.2:c.524G>T
|
NP_001138944.1:p.Gly175Val
|
|
|
NM_001308013.1:c.236G>T
|
NP_001294942.1:p.Gly79Val
|
|
|
NM_144612.6:c.3857G>T
|
NP_653213.6:p.Gly1286Val
|
|
|
XM_006722388.2:c.656G>T
|
XP_006722451.1:p.Gly219Val
|
|
|
XM_006722389.2:c.524G>T
|
XP_006722452.1:p.Gly175Val
|
|
|
XM_006722390.2:c.524G>T
|
XP_006722453.1:p.Gly175Val
|
|
|
XM_006722391.2:c.656G>T
|
XP_006722454.1:p.Gly219Val
|
|
|
XM_011525803.1:c.3857G>T
|
XP_011524105.1:p.Gly1286Val
|
|
|
XM_011525804.1:c.2018G>T
|
XP_011524106.1:p.Gly673Val
|
|
|
XM_011525805.1:c.521G>T
|
XP_011524107.1:p.Gly174Val
|
|
|
XM_011525806.1:c.236G>T
|
XP_011524108.1:p.Gly79Val
|
|
|
XM_011525807.1:c.236G>T
|
XP_011524109.1:p.Gly79Val
|
|
|
XM_011525809.1:c.236G>T
|
XP_011524111.1:p.Gly79Val
|
|
|
XM_006722388.3:c.656G>T
|
XP_006722451.1:p.Gly219Val
|
|
|
XM_006722389.3:c.524G>T
|
XP_006722452.1:p.Gly175Val
|
|
|
XM_006722390.3:c.524G>T
|
XP_006722453.1:p.Gly175Val
|
|
|
XM_006722391.3:c.656G>T
|
XP_006722454.1:p.Gly219Val
|
|
|
XM_011525804.2:c.2018G>T
|
XP_011524106.1:p.Gly673Val
|
|
|
XM_017025548.1:c.3239G>T
|
XP_016881037.1:p.Gly1080Val
|
|
|
XM_024451084.1:c.2339G>T
|
XP_024306852.1:p.Gly780Val
|
|
|
XM_024451085.1:c.521G>T
|
XP_024306853.1:p.Gly174Val
|
|
|
XM_024451086.1:c.236G>T
|
XP_024306854.1:p.Gly79Val
|
|
|
XM_024451087.1:c.236G>T
|
XP_024306855.1:p.Gly79Val
|
|
|
XM_024451088.1:c.236G>T
|
XP_024306856.1:p.Gly79Val
|
|
|
NM_001145472.3:c.524G>T
|
NP_001138944.1:p.Gly175Val
|
|
|
NM_001308013.2:c.236G>T
|
NP_001294942.1:p.Gly79Val
|
|
|
NM_001384474.1:c.3857G>T
MANE Select
|
NP_001371403.1:p.Gly1286Val
|
|
|
NM_144612.7:c.3857G>T
|
NP_653213.6:p.Gly1286Val
|
|
