|
NM_022124.6:c.2767G>A
MANE Select
|
NP_071407.4:p.Gly923Ser
|
|
ENST00000224721.12:c.2767G>A
MANE Select
|
ENSP00000224721.9:p.Gly923Ser
|
|
NM_001171930.1:c.2767G>A
|
NP_001165401.1:p.Gly923Ser
|
|
NM_001171930.2:c.2767G>A
|
NP_001165401.1:p.Gly923Ser
|
|
NM_001171931.1:c.2767G>A
|
NP_001165402.1:p.Gly923Ser
|
|
NM_001171931.2:c.2767G>A
|
NP_001165402.1:p.Gly923Ser
|
|
NM_022124.5:c.2767G>A
|
NP_071407.4:p.Gly923Ser
|
|
ENST00000224721.10:c.2782G>A
|
ENSP00000224721.8:p.Gly928Ser
|
|
ENST00000299366.11:c.2767G>A
|
ENSP00000299366.8:p.Gly923Ser
|
|
ENST00000398809.8:c.2767G>A
|
ENSP00000381789.5:p.Gly923Ser
|
|
ENST00000398809.9:c.2767G>A
|
ENSP00000381789.5:p.Gly923Ser
|
|
ENST00000442677.3:c.1542G>A
|
|
|
ENST00000442677.4:c.2767G>A
|
ENSP00000388894.3:p.Gly923Ser
|
|
ENST00000466757.7:c.2198G>A
|
|
|
ENST00000466757.8:c.2198G>A
|
|
|
ENST00000616684.4:c.2767G>A
|
ENSP00000482036.2:p.Gly923Ser
|
|
ENST00000622827.4:c.2767G>A
|
ENSP00000483211.1:p.Gly923Ser
|
|
XM_006717940.2:c.2962G>A
|
XP_006718003.1:p.Gly988Ser
|
|
XM_006717942.2:c.2896G>A
|
XP_006718005.1:p.Gly966Ser
|
|
XM_011540039.1:c.2962G>A
|
XP_011538341.1:p.Gly988Ser
|
|
XM_011540040.1:c.2956G>A
|
XP_011538342.1:p.Gly986Ser
|
|
XM_011540041.1:c.2902G>A
|
XP_011538343.1:p.Gly968Ser
|
|
XM_011540042.1:c.2962G>A
|
XP_011538344.1:p.Gly988Ser
|
|
XM_011540043.1:c.2962G>A
|
XP_011538345.1:p.Gly988Ser
|
|
XM_011540044.1:c.2827G>A
|
XP_011538346.1:p.Gly943Ser
|
|
XM_011540045.1:c.2962G>A
|
XP_011538347.1:p.Gly988Ser
|
|
XM_011540046.1:c.2422G>A
|
XP_011538348.1:p.Gly808Ser
|
|
XM_011540047.1:c.1780G>A
|
XP_011538349.1:p.Gly594Ser
|
|
XM_011540048.1:c.2962G>A
|
XP_011538350.1:p.Gly988Ser
|
|
XM_011540049.1:c.2962G>A
|
XP_011538351.1:p.Gly988Ser
|
|
XM_011540050.1:c.2962G>A
|
XP_011538352.1:p.Gly988Ser
|
|
XM_011540051.1:c.2962G>A
|
XP_011538353.1:p.Gly988Ser
|
|
XM_011540053.1:c.2962G>A
|
XP_011538355.1:p.Gly988Ser
|
|
XM_011540054.1:c.2902G>A
|
XP_011538356.1:p.Gly968Ser
|
|
XR_945796.1:n.3205G>A
|
|
|
XR_946052.1:n.83-349C>T
|
|
