|
ENST00000395796.8:c.*616G=
|
ENSP00000379142.4:n.*616G=
|
|
|
ENST00000616242.5:c.618G=
|
ENSP00000482149.2:p.Thr206=
|
|
|
ENST00000682635.1:n.1104G=
|
|
|
|
ENST00000345378.7:c.621G=
|
ENSP00000223366.2:p.Thr207=
|
|
|
ENST00000403799.8:c.618G=
MANE Select
|
ENSP00000384247.3:p.Thr206=
|
|
|
ENST00000671824.1:c.618G=
|
ENSP00000500264.1:p.Thr206=
|
|
|
ENST00000673284.1:c.618G=
|
ENSP00000499852.1:p.Thr206=
|
|
|
ENST00000345378.6:c.621G=
|
ENSP00000223366.2:p.Thr207=
|
|
|
ENST00000395796.7:c.615G=
|
ENSP00000379142.3:p.Thr205=
|
|
|
ENST00000403799.7:c.618G=
|
ENSP00000384247.3:p.Thr206=
|
|
|
ENST00000437084.1:c.567G=
|
ENSP00000402840.1:p.Thr189=
|
|
|
ENST00000616242.4:c.615G=
|
ENSP00000482149.1:p.Thr205=
|
|
|
NM_000162.3:c.618G=
|
NP_000153.1:p.Thr206=
|
|
|
NM_033507.1:c.621G=
|
NP_277042.1:p.Thr207=
|
|
|
NM_033508.1:c.615G=
|
NP_277043.1:p.Thr205=
|
|
|
NM_000162.4:c.618G=
|
NP_000153.1:p.Thr206=
|
|
|
NM_001354800.1:c.618G=
|
NP_001341729.1:p.Thr206=
|
|
|
NM_033507.2:c.621G=
|
NP_277042.1:p.Thr207=
|
|
|
NM_033508.2:c.615G=
|
NP_277043.1:p.Thr205=
|
|
|
NM_000162.5:c.618G=
MANE Select
|
NP_000153.1:p.Thr206=
|
|
|
NM_033507.3:c.621G=
|
NP_277042.1:p.Thr207=
|
|
|
NM_033508.3:c.615G=
|
NP_277043.1:p.Thr205=
|
|
