ENST00000698254.1:c.751G>T
|
ENSP00000513629.1:p.Gly251Cys
|
|
ENST00000698255.1:c.1171G>T
|
ENSP00000513630.1:p.Gly391Cys
|
|
ENST00000698256.1:c.688G>T
|
|
|
ENST00000698257.1:n.640G>T
|
|
|
ENST00000698258.1:n.206G>T
|
|
|
ENST00000698259.1:n.46G>T
|
|
|
ENST00000265686.8:c.1222G>T
MANE Select
|
ENSP00000265686.3:p.Gly408Cys
|
|
ENST00000265686.7:c.1222G>T
|
ENSP00000265686.3:p.Gly408Cys
|
|
ENST00000525516.1:n.16G>T
|
|
|
ENST00000525724.5:n.534G>T
|
|
|
ENST00000528981.5:c.374G>T
|
|
|
ENST00000529364.1:c.633G>T
|
|
|
ENST00000532635.5:c.574G>T
|
ENSP00000434407.1:p.Gly192Cys
|
|
ENST00000533005.5:n.258G>T
|
|
|
NM_006019.3:c.1222G>T
|
NP_006010.2:p.Gly408Cys
|
|
NM_006053.3:c.574G>T
|
NP_006044.1:p.Gly192Cys
|
|
XM_005273709.2:c.1222G>T
|
XP_005273766.1:p.Gly408Cys
|
|
XM_011544726.1:c.1222G>T
|
XP_011543028.1:p.Gly408Cys
|
|
XM_011544727.1:c.1222G>T
|
XP_011543029.1:p.Gly408Cys
|
|
XM_011544728.1:c.1222G>T
|
XP_011543030.1:p.Gly408Cys
|
|
XM_011544729.1:c.1238G>T
|
XP_011543031.1:p.Gly413Val
|
|
XR_949754.1:n.1226G>T
|
|
|
NM_001351059.1:c.328G>T
|
NP_001337988.1:p.Gly110Cys
|
|
XM_024448320.1:c.1238G>T
|
XP_024304088.1:p.Gly413Val
|
|
XM_024448321.1:c.1238G>T
|
XP_024304089.1:p.Gly413Val
|
|
XM_024448322.1:c.1238G>T
|
XP_024304090.1:p.Gly413Val
|
|
XM_024448323.1:c.1238G>T
|
XP_024304091.1:p.Gly413Val
|
|
XM_024448324.1:c.1238G>T
|
XP_024304092.1:p.Gly413Val
|
|
XR_001747721.2:n.1346G>T
|
|
|
XR_001747722.1:n.1359G>T
|
|
|
XR_001747723.2:n.1359G>T
|
|
|
XR_002957115.1:n.1360G>T
|
|
|
NM_006019.4:c.1222G>T
MANE Select
|
NP_006010.2:p.Gly408Cys
|
|
NM_001351059.2:c.328G>T
|
NP_001337988.1:p.Gly110Cys
|
|
NM_006053.4:c.574G>T
|
NP_006044.1:p.Gly192Cys
|
|