|
ENST00000395796.8:c.*1026G>C
|
ENSP00000379142.4:n.*1026G>C
|
|
|
ENST00000616242.5:c.*148G>C
|
ENSP00000482149.2:n.*148G>C
|
|
|
ENST00000683378.1:n.254G>C
|
|
|
|
ENST00000336642.9:c.62G>C
|
ENSP00000338009.5:p.Gly21Ala
|
|
|
ENST00000345378.7:c.1031G>C
|
ENSP00000223366.2:p.Gly344Ala
|
|
|
ENST00000403799.8:c.1028G>C
MANE Select
|
ENSP00000384247.3:p.Gly343Ala
|
|
|
ENST00000671824.1:c.1091G>C
|
ENSP00000500264.1:p.Gly364Ala
|
|
|
ENST00000672743.1:n.40G>C
|
|
|
|
ENST00000673284.1:c.1028G>C
|
ENSP00000499852.1:p.Gly343Ala
|
|
|
ENST00000336642.8:c.80G>C
|
ENSP00000338009.4:p.Gly27Ala
|
|
|
ENST00000345378.6:c.1031G>C
|
ENSP00000223366.2:p.Gly344Ala
|
|
|
ENST00000395796.7:c.1025G>C
|
ENSP00000379142.3:p.Gly342Ala
|
|
|
ENST00000403799.7:c.1028G>C
|
ENSP00000384247.3:p.Gly343Ala
|
|
|
ENST00000437084.1:c.977G>C
|
ENSP00000402840.1:p.Gly326Ala
|
|
|
ENST00000459642.1:n.408G>C
|
|
|
|
ENST00000473353.1:n.326G>C
|
|
|
|
ENST00000616242.4:c.1025G>C
|
ENSP00000482149.1:p.Gly342Ala
|
|
|
NM_000162.3:c.1028G>C
|
NP_000153.1:p.Gly343Ala
|
|
|
NM_033507.1:c.1031G>C
|
NP_277042.1:p.Gly344Ala
|
|
|
NM_033508.1:c.1025G>C
|
NP_277043.1:p.Gly342Ala
|
|
|
NM_000162.4:c.1028G>C
|
NP_000153.1:p.Gly343Ala
|
|
|
NM_001354800.1:c.1028G>C
|
NP_001341729.1:p.Gly343Ala
|
|
|
NM_001354801.1:c.17G>C
|
NP_001341730.1:p.Gly6Ala
|
|
|
NM_001354802.1:c.-113G>C
|
NP_001341731.1:n.-113G>C
|
|
|
NM_001354803.1:c.62G>C
|
NP_001341732.1:p.Gly21Ala
|
|
|
NM_033507.2:c.1031G>C
|
NP_277042.1:p.Gly344Ala
|
|
|
NM_033508.2:c.1025G>C
|
NP_277043.1:p.Gly342Ala
|
|
|
XM_024446707.1:c.-113G>C
|
XP_024302475.1:n.-113G>C
|
|
|
NM_000162.5:c.1028G>C
MANE Select
|
NP_000153.1:p.Gly343Ala
|
|
|
NM_033507.3:c.1031G>C
|
NP_277042.1:p.Gly344Ala
|
|
|
NM_033508.3:c.1025G>C
|
NP_277043.1:p.Gly342Ala
|
|
|
NM_001354803.2:c.62G>C
|
NP_001341732.1:p.Gly21Ala
|
|
