ENST00000264595.7:c.581T>C
MANE Select
|
ENSP00000264595.2:p.Ile194Thr
|
|
ENST00000264595.6:c.581T>C
|
ENSP00000264595.2:p.Ile194Thr
|
|
ENST00000502310.5:c.236T>C
|
ENSP00000423798.1:p.Ile79Thr
|
|
ENST00000506853.5:n.615T>C
|
|
|
ENST00000510635.1:c.277T>C
|
|
|
ENST00000510955.5:n.502T>C
|
|
|
NM_000027.3:c.581T>C
|
NP_000018.2:p.Ile194Thr
|
|
NM_001171988.1:c.581T>C
|
NP_001165459.1:p.Ile194Thr
|
|
NR_033655.1:n.709T>C
|
|
|
XM_006714123.2:c.581T>C
|
XP_006714186.1:p.Ile194Thr
|
|
XR_001741155.2:n.675T>C
|
|
|
NM_000027.4:c.581T>C
MANE Select
|
NP_000018.2:p.Ile194Thr
|
|
NM_001171988.2:c.581T>C
|
NP_001165459.1:p.Ile194Thr
|
|
NR_033655.2:n.643T>C
|
|
|