ENST00000698254.1:c.880G>T
|
ENSP00000513629.1:p.Gly294Cys
|
|
ENST00000698255.1:c.1300G>T
|
ENSP00000513630.1:p.Gly434Cys
|
|
ENST00000698256.1:c.817G>T
|
|
|
ENST00000698257.1:n.769G>T
|
|
|
ENST00000698258.1:n.409G>T
|
|
|
ENST00000698259.1:n.175G>T
|
|
|
ENST00000265686.8:c.1351G>T
MANE Select
|
ENSP00000265686.3:p.Gly451Cys
|
|
ENST00000265686.7:c.1351G>T
|
ENSP00000265686.3:p.Gly451Cys
|
|
ENST00000525516.1:n.145G>T
|
|
|
ENST00000525724.5:n.663G>T
|
|
|
ENST00000528981.5:c.503G>T
|
|
|
ENST00000529364.1:c.762G>T
|
|
|
ENST00000532635.5:c.703G>T
|
ENSP00000434407.1:p.Gly235Cys
|
|
ENST00000533005.5:n.387G>T
|
|
|
NM_006019.3:c.1351G>T
|
NP_006010.2:p.Gly451Cys
|
|
NM_006053.3:c.703G>T
|
NP_006044.1:p.Gly235Cys
|
|
XM_005273709.2:c.1351G>T
|
XP_005273766.1:p.Gly451Cys
|
|
XM_011544726.1:c.1351G>T
|
XP_011543028.1:p.Gly451Cys
|
|
XM_011544727.1:c.1351G>T
|
XP_011543029.1:p.Gly451Cys
|
|
XM_011544728.1:c.1351G>T
|
XP_011543030.1:p.Gly451Cys
|
|
XM_011544729.1:c.1367G>T
|
XP_011543031.1:p.Gly456Val
|
|
XR_949754.1:n.1355G>T
|
|
|
NM_001351059.1:c.457G>T
|
NP_001337988.1:p.Gly153Cys
|
|
XM_024448320.1:c.1367G>T
|
XP_024304088.1:p.Gly456Val
|
|
XM_024448321.1:c.1367G>T
|
XP_024304089.1:p.Gly456Val
|
|
XM_024448322.1:c.1367G>T
|
XP_024304090.1:p.Gly456Val
|
|
XM_024448323.1:c.1367G>T
|
XP_024304091.1:p.Gly456Val
|
|
XM_024448324.1:c.1367G>T
|
XP_024304092.1:p.Gly456Val
|
|
XR_001747721.2:n.1475G>T
|
|
|
XR_001747722.1:n.1488G>T
|
|
|
XR_001747723.2:n.1488G>T
|
|
|
XR_002957115.1:n.1489G>T
|
|
|
NM_006019.4:c.1351G>T
MANE Select
|
NP_006010.2:p.Gly451Cys
|
|
NM_001351059.2:c.457G>T
|
NP_001337988.1:p.Gly153Cys
|
|
NM_006053.4:c.703G>T
|
NP_006044.1:p.Gly235Cys
|
|