ENST00000651671.1:c.6402C>A
MANE Select
|
ENSP00000498587.1:p.Thr2134=
|
|
ENST00000679595.1:c.*1442C>A
|
ENSP00000506241.1:n.*1442C>A
|
|
ENST00000679969.1:n.2998C>A
|
|
|
ENST00000680003.1:n.2734C>A
|
|
|
ENST00000680133.1:c.6288C>A
|
ENSP00000505319.1:p.Thr2096=
|
|
ENST00000680218.1:c.6282C>A
|
ENSP00000505339.1:p.Thr2094=
|
|
ENST00000680668.1:c.6288C>A
|
ENSP00000506336.1:p.Thr2096=
|
|
ENST00000680778.1:c.3999C>A
|
ENSP00000506033.1:p.Thr1333=
|
|
ENST00000680924.1:c.*3802C>A
|
ENSP00000506031.1:n.*3802C>A
|
|
ENST00000681135.1:c.*4011C>A
|
ENSP00000506636.1:n.*4011C>A
|
|
ENST00000681298.1:n.4507C>A
|
|
|
ENST00000681454.1:c.*5638C>A
|
ENSP00000505763.1:n.*5638C>A
|
|
ENST00000277541.6:c.6402C>A
|
ENSP00000277541.6:p.Thr2134=
|
|
NM_017617.3:c.6402C>A
|
NP_060087.3:p.Thr2134=
|
|
XM_011518717.1:c.5703C>A
|
XP_011517019.1:p.Thr1901=
|
|
NM_017617.5:c.6402C>A
MANE Select
|
NP_060087.3:p.Thr2134=
|
|
XM_011518717.2:c.5679C>A
|
XP_011517019.2:p.Thr1893=
|
|