ENST00000681993.1:n.459T>A
|
|
|
ENST00000682295.1:c.171T>A
|
ENSP00000507499.1:p.Gly57=
|
|
ENST00000682303.1:c.*2693T>A
|
ENSP00000508325.1:n.*2693T>A
|
|
ENST00000682308.1:c.2907T>A
|
ENSP00000507056.1:p.Gly969=
|
|
ENST00000682480.1:c.2907T>A
|
ENSP00000508344.1:p.Gly969=
|
|
ENST00000682546.1:c.2904T>A
|
ENSP00000508188.1:p.Gly968=
|
|
ENST00000682585.1:c.2907T>A
|
ENSP00000506885.1:p.Gly969=
|
|
ENST00000682595.1:n.3491T>A
|
|
|
ENST00000682607.1:c.1325T>A
|
|
|
ENST00000682779.1:c.2898T>A
|
ENSP00000507947.1:p.Gly966=
|
|
ENST00000682845.1:n.2009T>A
|
|
|
ENST00000682885.1:c.2862T>A
|
ENSP00000508036.1:p.Gly954=
|
|
ENST00000682933.1:n.2981T>A
|
|
|
ENST00000683072.1:n.3491T>A
|
|
|
ENST00000683080.1:n.526T>A
|
|
|
ENST00000683125.1:c.3015T>A
|
ENSP00000507939.1:p.Gly1005=
|
|
ENST00000683213.1:c.2910T>A
|
ENSP00000507751.1:p.Gly970=
|
|
ENST00000683220.1:c.2937T>A
|
ENSP00000507151.1:p.Gly979=
|
|
ENST00000683236.1:c.237T>A
|
ENSP00000506891.1:n.237T>A
|
|
ENST00000683329.1:n.3710T>A
|
|
|
ENST00000683346.1:c.*2782T>A
|
ENSP00000507458.1:n.*2782T>A
|
|
ENST00000683409.1:n.1514T>A
|
|
|
ENST00000683459.1:n.3494T>A
|
|
|
ENST00000683590.1:c.2897-5830T>A
|
ENSP00000506820.1:n.2897-5830T>A
|
|
ENST00000683623.1:c.2814T>A
|
ENSP00000507702.1:p.Gly938=
|
|
ENST00000683645.1:n.3458T>A
|
|
|
ENST00000683796.1:c.*2779T>A
|
ENSP00000508221.1:n.*2779T>A
|
|
ENST00000683802.1:n.5832T>A
|
|
|
ENST00000683833.1:c.2898T>A
|
ENSP00000506852.1:p.Gly966=
|
|
ENST00000683994.1:c.2907T>A
|
ENSP00000507181.1:p.Gly969=
|
|
ENST00000684290.1:c.*443T>A
|
ENSP00000507243.1:n.*443T>A
|
|
ENST00000684306.1:c.*2820T>A
|
ENSP00000508384.1:n.*2820T>A
|
|
ENST00000684341.1:n.2927T>A
|
|
|
ENST00000684383.1:c.*2545T>A
|
ENSP00000506863.1:n.*2545T>A
|
|
ENST00000684619.1:c.*2779T>A
|
ENSP00000508088.1:n.*2779T>A
|
|
ENST00000684705.1:n.28T>A
|
|
|
ENST00000684743.1:n.3938T>A
|
|
|
ENST00000260665.12:c.2907T>A
MANE Select
|
ENSP00000260665.7:p.Gly969=
|
|
ENST00000260665.11:c.2907T>A
|
ENSP00000260665.7:p.Gly969=
|
|
NM_133259.3:c.2907T>A
|
NP_573566.2:p.Gly969=
|
|
XM_006711915.2:c.2829T>A
|
XP_006711978.1:p.Gly943=
|
|
XM_006711916.2:c.2907T>A
|
XP_006711979.1:p.Gly969=
|
|
XM_011532473.1:c.2907T>A
|
XP_011530775.1:p.Gly969=
|
|
XM_011532474.1:c.2907T>A
|
XP_011530776.1:p.Gly969=
|
|
XM_006711916.3:c.2907T>A
|
XP_006711979.1:p.Gly969=
|
|
XM_017003117.1:c.2829T>A
|
XP_016858606.1:p.Gly943=
|
|
XR_002958896.1:n.2949T>A
|
|
|
NM_133259.4:c.2907T>A
MANE Select
|
NP_573566.2:p.Gly969=
|
|