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ENST00000261769.10:c.2452G=
MANE Select
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ENSP00000261769.4:p.Ala818=
|
|
|
ENST00000261769.9:c.2452G=
|
ENSP00000261769.4:p.Ala818=
|
|
|
ENST00000422392.6:c.2269G=
|
ENSP00000414946.2:p.Ala757=
|
|
|
ENST00000562118.1:n.670G=
|
|
|
|
ENST00000562836.5:n.2523G=
|
|
|
|
ENST00000566510.5:c.*1118G=
|
ENSP00000458139.1:n.*1118G=
|
|
|
ENST00000566612.5:c.*692G=
|
ENSP00000454782.1:n.*692G=
|
|
|
ENST00000611625.4:c.2515G=
|
ENSP00000481063.1:p.Ala839=
|
|
|
ENST00000612417.4:c.1854-889G=
|
ENSP00000478360.1:n.1854-889G=
|
|
|
ENST00000621016.4:c.1866-901G=
|
ENSP00000480664.1:n.1866-901G=
|
|
|
NM_004360.3:c.2452G= , LRG_301t1:c.2452G=
|
NP_004351.1:p.Ala818=
|
|
|
XM_011523488.1:c.1717G=
|
XP_011521790.1:p.Ala573=
|
|
|
XM_011523489.1:c.1717G=
|
XP_011521791.1:p.Ala573=
|
|
|
NM_001317184.1:c.2269G=
|
NP_001304113.1:p.Ala757=
|
|
|
NM_001317185.1:c.904G=
|
NP_001304114.1:p.Ala302=
|
|
|
NM_001317186.1:c.487G=
|
NP_001304115.1:p.Ala163=
|
|
|
NM_004360.4:c.2452G=
|
NP_004351.1:p.Ala818=
|
|
|
NM_004360.5:c.2452G=
MANE Select
|
NP_004351.1:p.Ala818=
|
|
|
NM_001317184.2:c.2269G=
|
NP_001304113.1:p.Ala757=
|
|
|
NM_001317185.2:c.904G=
|
NP_001304114.1:p.Ala302=
|
|
|
NM_001317186.2:c.487G=
|
NP_001304115.1:p.Ala163=
|
|
