ENST00000651671.1:c.7398G>A
MANE Select
|
ENSP00000498587.1:p.Thr2466=
|
|
ENST00000679595.1:c.*2438G>A
|
ENSP00000506241.1:n.*2438G>A
|
|
ENST00000679969.1:n.3994G>A
|
|
|
ENST00000680003.1:n.3730G>A
|
|
|
ENST00000680133.1:c.7284G>A
|
ENSP00000505319.1:p.Thr2428=
|
|
ENST00000680218.1:c.7278G>A
|
ENSP00000505339.1:p.Thr2426=
|
|
ENST00000680668.1:c.7284G>A
|
ENSP00000506336.1:p.Thr2428=
|
|
ENST00000680778.1:c.4995G>A
|
ENSP00000506033.1:p.Thr1665=
|
|
ENST00000680924.1:c.*4798G>A
|
ENSP00000506031.1:n.*4798G>A
|
|
ENST00000681135.1:c.*5007G>A
|
ENSP00000506636.1:n.*5007G>A
|
|
ENST00000681298.1:n.5503G>A
|
|
|
ENST00000681454.1:c.*6634G>A
|
ENSP00000505763.1:n.*6634G>A
|
|
ENST00000277541.6:c.7398G>A
|
ENSP00000277541.6:p.Thr2466=
|
|
NM_017617.3:c.7398G>A
|
NP_060087.3:p.Thr2466=
|
|
XM_011518717.1:c.6699G>A
|
XP_011517019.1:p.Thr2233=
|
|
NM_017617.5:c.7398G>A
MANE Select
|
NP_060087.3:p.Thr2466=
|
|
XM_011518717.2:c.6675G>A
|
XP_011517019.2:p.Thr2225=
|
|