ENST00000645828.1:n.2751G>T
|
|
|
ENST00000651671.1:c.4944G>T
MANE Select
|
ENSP00000498587.1:p.Val1648=
|
|
ENST00000679595.1:c.4944G>T
|
ENSP00000506241.1:p.Val1648=
|
|
ENST00000680133.1:c.4830G>T
|
ENSP00000505319.1:p.Val1610=
|
|
ENST00000680218.1:c.4824G>T
|
ENSP00000505339.1:p.Val1608=
|
|
ENST00000680668.1:c.4830G>T
|
ENSP00000506336.1:p.Val1610=
|
|
ENST00000680778.1:c.2541G>T
|
ENSP00000506033.1:p.Val847=
|
|
ENST00000680924.1:c.*2344G>T
|
ENSP00000506031.1:n.*2344G>T
|
|
ENST00000681135.1:c.*2553G>T
|
ENSP00000506636.1:n.*2553G>T
|
|
ENST00000681298.1:n.1757G>T
|
|
|
ENST00000681454.1:c.*4180G>T
|
ENSP00000505763.1:n.*4180G>T
|
|
ENST00000277541.6:c.4944G>T
|
ENSP00000277541.6:p.Val1648=
|
|
ENST00000494783.1:n.99G>T
|
|
|
NM_017617.3:c.4944G>T
|
NP_060087.3:p.Val1648=
|
|
XM_011518717.1:c.4245G>T
|
XP_011517019.1:p.Val1415=
|
|
NM_017617.5:c.4944G>T
MANE Select
|
NP_060087.3:p.Val1648=
|
|
XM_011518717.2:c.4221G>T
|
XP_011517019.2:p.Val1407=
|
|