ENST00000645828.1:n.2824G>T
|
|
|
ENST00000651671.1:c.5017G>T
MANE Select
|
ENSP00000498587.1:p.Gly1673Cys
|
|
ENST00000679595.1:c.5017G>T
|
ENSP00000506241.1:p.Gly1673Cys
|
|
ENST00000680133.1:c.4903G>T
|
ENSP00000505319.1:p.Gly1635Cys
|
|
ENST00000680218.1:c.4897G>T
|
ENSP00000505339.1:p.Gly1633Cys
|
|
ENST00000680668.1:c.4903G>T
|
ENSP00000506336.1:p.Gly1635Cys
|
|
ENST00000680778.1:c.2614G>T
|
ENSP00000506033.1:p.Gly872Cys
|
|
ENST00000680924.1:c.*2417G>T
|
ENSP00000506031.1:n.*2417G>T
|
|
ENST00000681135.1:c.*2626G>T
|
ENSP00000506636.1:n.*2626G>T
|
|
ENST00000681298.1:n.1830G>T
|
|
|
ENST00000681454.1:c.*4253G>T
|
ENSP00000505763.1:n.*4253G>T
|
|
ENST00000277541.6:c.5017G>T
|
ENSP00000277541.6:p.Gly1673Cys
|
|
ENST00000494783.1:n.172G>T
|
|
|
NM_017617.3:c.5017G>T
|
NP_060087.3:p.Gly1673Cys
|
|
XM_011518717.1:c.4318G>T
|
XP_011517019.1:p.Gly1440Cys
|
|
NM_017617.5:c.5017G>T
MANE Select
|
NP_060087.3:p.Gly1673Cys
|
|
XM_011518717.2:c.4294G>T
|
XP_011517019.2:p.Gly1432Cys
|
|