ENST00000645828.1:n.2721G>A
|
|
|
ENST00000651671.1:c.4914G>A
MANE Select
|
ENSP00000498587.1:p.Trp1638Ter
|
|
ENST00000679595.1:c.4914G>A
|
ENSP00000506241.1:p.Trp1638Ter
|
|
ENST00000680133.1:c.4800G>A
|
ENSP00000505319.1:p.Trp1600Ter
|
|
ENST00000680218.1:c.4794G>A
|
ENSP00000505339.1:p.Trp1598Ter
|
|
ENST00000680668.1:c.4800G>A
|
ENSP00000506336.1:p.Trp1600Ter
|
|
ENST00000680778.1:c.2511G>A
|
ENSP00000506033.1:p.Trp837Ter
|
|
ENST00000680924.1:c.*2314G>A
|
ENSP00000506031.1:n.*2314G>A
|
|
ENST00000681135.1:c.*2523G>A
|
ENSP00000506636.1:n.*2523G>A
|
|
ENST00000681298.1:n.1727G>A
|
|
|
ENST00000681454.1:c.*4150G>A
|
ENSP00000505763.1:n.*4150G>A
|
|
ENST00000277541.6:c.4914G>A
|
ENSP00000277541.6:p.Trp1638Ter
|
|
ENST00000494783.1:n.69G>A
|
|
|
NM_017617.3:c.4914G>A
|
NP_060087.3:p.Trp1638Ter
|
|
XM_011518717.1:c.4215G>A
|
XP_011517019.1:p.Trp1405Ter
|
|
NM_017617.5:c.4914G>A
MANE Select
|
NP_060087.3:p.Trp1638Ter
|
|
XM_011518717.2:c.4191G>A
|
XP_011517019.2:p.Trp1397Ter
|
|