ENST00000645828.1:n.2459G>C
|
|
|
ENST00000651671.1:c.4652G>C
MANE Select
|
ENSP00000498587.1:p.Ser1551Thr
|
|
ENST00000679595.1:c.4652G>C
|
ENSP00000506241.1:p.Ser1551Thr
|
|
ENST00000680133.1:c.4538G>C
|
ENSP00000505319.1:p.Ser1513Thr
|
|
ENST00000680218.1:c.4532G>C
|
ENSP00000505339.1:p.Ser1511Thr
|
|
ENST00000680668.1:c.4538G>C
|
ENSP00000506336.1:p.Ser1513Thr
|
|
ENST00000680778.1:c.2249G>C
|
ENSP00000506033.1:p.Ser750Thr
|
|
ENST00000680924.1:c.*2052G>C
|
ENSP00000506031.1:n.*2052G>C
|
|
ENST00000681135.1:c.*2261G>C
|
ENSP00000506636.1:n.*2261G>C
|
|
ENST00000681298.1:n.1465G>C
|
|
|
ENST00000681454.1:c.*3888G>C
|
ENSP00000505763.1:n.*3888G>C
|
|
ENST00000277541.6:c.4652G>C
|
ENSP00000277541.6:p.Ser1551Thr
|
|
NM_017617.3:c.4652G>C
|
NP_060087.3:p.Ser1551Thr
|
|
XM_011518717.1:c.3953G>C
|
XP_011517019.1:p.Ser1318Thr
|
|
NM_017617.5:c.4652G>C
MANE Select
|
NP_060087.3:p.Ser1551Thr
|
|
XM_011518717.2:c.3929G>C
|
XP_011517019.2:p.Ser1310Thr
|
|