ENST00000684169.1:c.983G>C
|
ENSP00000506849.1:p.Ser328Thr
|
|
ENST00000392386.8:c.983G>C
MANE Select
|
ENSP00000376188.2:p.Ser328Thr
|
|
ENST00000392386.7:c.983G>C
|
ENSP00000376188.2:p.Ser328Thr
|
|
ENST00000597131.1:c.447+1G>C
|
|
|
NM_004750.4:c.983G>C
|
NP_004741.1:p.Ser328Thr
|
|
XM_011528422.1:c.917G>C
|
XP_011526724.1:p.Ser306Thr
|
|
XM_011528423.1:c.983G>C
|
XP_011526725.1:p.Ser328Thr
|
|
XM_011528424.1:c.917G>C
|
XP_011526726.1:p.Ser306Thr
|
|
XM_011528422.2:c.917G>C
|
XP_011526724.1:p.Ser306Thr
|
|
XM_011528423.2:c.983G>C
|
XP_011526725.1:p.Ser328Thr
|
|
XM_011528424.3:c.917G>C
|
XP_011526726.1:p.Ser306Thr
|
|
NM_004750.5:c.983G>C
MANE Select
|
NP_004741.1:p.Ser328Thr
|
|