|
NM_178821.3:c.1116G>T
MANE Select
|
NP_849143.1:p.Trp372Cys
|
|
ENST00000309931.3:c.1116G>T
MANE Select
|
ENSP00000311899.2:p.Trp372Cys
|
|
NM_001330004.1:c.1071G>T
|
NP_001316933.1:p.Trp357Cys
|
|
NM_001330004.2:c.1071G>T
|
NP_001316933.1:p.Trp357Cys
|
|
NM_178821.1:c.1116G>T
|
NP_849143.1:p.Trp372Cys
|
|
NM_178821.2:c.1116G>T
|
NP_849143.1:p.Trp372Cys
|
|
NR_138459.1:n.1646G>T
|
|
|
NR_138459.2:n.1391G>T
|
|
|
ENST00000309931.2:c.1116G>T
|
ENSP00000311899.2:p.Trp372Cys
|
|
ENST00000373666.6:c.*222G>T
|
ENSP00000362770.2:n.*222G>T
|
|
XM_011510755.1:c.1071G>T
|
XP_011509057.1:p.Trp357Cys
|
|
XM_017003490.1:c.528G>T
|
XP_016858979.1:p.Trp176Cys
|