ENST00000270301.12:c.3315A>G
|
ENSP00000270301.6:p.Ala1105=
|
|
ENST00000401500.7:c.3330A>G
MANE Select
|
ENSP00000384792.1:p.Ala1110=
|
|
ENST00000587391.6:c.*3190A>G
|
ENSP00000465525.1:n.*3190A>G
|
|
ENST00000679357.1:c.1410A>G
|
|
|
ENST00000679598.1:c.95A>G
|
|
|
ENST00000679682.1:c.3315A>G
|
ENSP00000506226.1:p.Ala1105=
|
|
ENST00000679714.1:c.3324A>G
|
ENSP00000506627.1:p.Ala1108=
|
|
ENST00000679757.1:c.2979A>G
|
ENSP00000505158.1:p.Ala993=
|
|
ENST00000679858.1:c.*2712A>G
|
ENSP00000505655.1:n.*2712A>G
|
|
ENST00000680211.1:c.-70A>G
|
ENSP00000506102.1:n.-70A>G
|
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ENST00000680280.1:n.617A>G
|
|
|
ENST00000680349.1:n.1898A>G
|
|
|
ENST00000680403.1:c.3315A>G
|
ENSP00000505677.1:p.Ala1105=
|
|
ENST00000680564.1:c.3081A>G
|
ENSP00000505582.1:p.Ala1027=
|
|
ENST00000680590.1:c.*1710A>G
|
ENSP00000505350.1:n.*1710A>G
|
|
ENST00000680597.1:c.95A>G
|
|
|
ENST00000680739.1:c.345A>G
|
|
|
ENST00000680773.1:n.1831A>G
|
|
|
ENST00000680806.1:c.*2633A>G
|
ENSP00000506418.1:n.*2633A>G
|
|
ENST00000680997.1:n.1262A>G
|
|
|
ENST00000681608.1:n.863A>G
|
|
|
ENST00000681625.1:c.*662A>G
|
ENSP00000505555.1:n.*662A>G
|
|
ENST00000681648.1:n.629A>G
|
|
|
ENST00000270301.11:c.3315A>G
|
ENSP00000270301.6:p.Ala1105=
|
|
ENST00000401500.6:c.3330A>G
|
ENSP00000384792.1:p.Ala1110=
|
|
ENST00000587391.5:c.*3190A>G
|
ENSP00000465525.1:n.*3190A>G
|
|
NM_001083961.1:c.3330A>G
|
NP_001077430.1:p.Ala1110=
|
|
NM_173636.4:c.3315A>G
|
NP_775907.4:p.Ala1105=
|
|
XM_005258809.2:c.3219A>G
|
XP_005258866.1:p.Ala1073=
|
|
XM_011526837.1:c.3315A>G
|
XP_011525139.1:p.Ala1105=
|
|
XM_011526838.1:c.3081A>G
|
XP_011525140.1:p.Ala1027=
|
|
XM_011526839.1:c.2979A>G
|
XP_011525141.1:p.Ala993=
|
|
XM_011526840.1:c.2322A>G
|
XP_011525142.1:p.Ala774=
|
|
XM_011526841.1:c.1908A>G
|
XP_011525143.1:p.Ala636=
|
|
XM_011526842.1:c.1761A>G
|
XP_011525144.1:p.Ala587=
|
|
XM_011526843.1:c.1077A>G
|
XP_011525145.1:p.Ala359=
|
|
XM_011526844.1:c.1077A>G
|
XP_011525146.1:p.Ala359=
|
|
XM_011526840.2:c.2322A>G
|
XP_011525142.1:p.Ala774=
|
|
XM_011526841.2:c.1908A>G
|
XP_011525143.1:p.Ala636=
|
|
XM_011526844.2:c.1077A>G
|
XP_011525146.1:p.Ala359=
|
|
XM_017026665.1:c.3330A>G
|
XP_016882154.1:p.Ala1110=
|
|
NM_001083961.2:c.3330A>G
MANE Select
|
NP_001077430.1:p.Ala1110=
|
|
NM_173636.5:c.3315A>G
|
NP_775907.4:p.Ala1105=
|
|