ENST00000391944.8:c.2173G=
|
ENSP00000375808.4:p.Ala725=
|
|
ENST00000682414.1:c.2173G=
|
ENSP00000507019.1:p.Ala725=
|
|
ENST00000682508.1:n.2202G=
|
|
|
ENST00000684218.1:c.*1431G=
|
ENSP00000507804.1:n.*1431G=
|
|
ENST00000684264.1:n.1729G=
|
|
|
ENST00000684407.1:c.2050G=
|
ENSP00000507775.1:p.Ala684=
|
|
ENST00000684458.1:c.*659G=
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ENSP00000508260.1:n.*659G=
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|
ENST00000684468.1:n.1885G=
|
|
|
ENST00000391945.10:c.2173G=
MANE Select
|
ENSP00000375809.4:p.Ala725=
|
|
ENST00000646507.1:n.2270G=
|
|
|
ENST00000391941.6:c.2101G=
|
ENSP00000375805.2:p.Ala701=
|
|
ENST00000391942.6:n.1344G=
|
|
|
ENST00000391944.7:c.1939G=
|
ENSP00000375808.3:p.Ala647=
|
|
ENST00000391945.8:c.2173G=
|
ENSP00000375809.3:p.Ala725=
|
|
ENST00000588652.5:n.2261G=
|
|
|
NM_000400.3:c.2173G= , LRG_461t1:c.2173G=
|
NP_000391.1:p.Ala725=
|
|
XM_011526611.1:c.2095G=
|
XP_011524913.1:p.Ala699=
|
|
XM_011526611.2:c.2095G=
|
XP_011524913.1:p.Ala699=
|
|
XM_017026467.1:c.2050G=
|
XP_016881956.1:p.Ala684=
|
|
XR_001753633.2:n.2220G=
|
|
|
XR_001753634.2:n.2156G=
|
|
|
NM_000400.4:c.2173G=
MANE Select
|
NP_000391.1:p.Ala725=
|
|