ENST00000645828.1:n.2730T>C
|
|
|
ENST00000651671.1:c.4923T>C
MANE Select
|
ENSP00000498587.1:p.Pro1641=
|
|
ENST00000679595.1:c.4923T>C
|
ENSP00000506241.1:p.Pro1641=
|
|
ENST00000680133.1:c.4809T>C
|
ENSP00000505319.1:p.Pro1603=
|
|
ENST00000680218.1:c.4803T>C
|
ENSP00000505339.1:p.Pro1601=
|
|
ENST00000680668.1:c.4809T>C
|
ENSP00000506336.1:p.Pro1603=
|
|
ENST00000680778.1:c.2520T>C
|
ENSP00000506033.1:p.Pro840=
|
|
ENST00000680924.1:c.*2323T>C
|
ENSP00000506031.1:n.*2323T>C
|
|
ENST00000681135.1:c.*2532T>C
|
ENSP00000506636.1:n.*2532T>C
|
|
ENST00000681298.1:n.1736T>C
|
|
|
ENST00000681454.1:c.*4159T>C
|
ENSP00000505763.1:n.*4159T>C
|
|
ENST00000277541.6:c.4923T>C
|
ENSP00000277541.6:p.Pro1641=
|
|
ENST00000494783.1:n.78T>C
|
|
|
NM_017617.3:c.4923T>C
|
NP_060087.3:p.Pro1641=
|
|
XM_011518717.1:c.4224T>C
|
XP_011517019.1:p.Pro1408=
|
|
NM_017617.5:c.4923T>C
MANE Select
|
NP_060087.3:p.Pro1641=
|
|
XM_011518717.2:c.4200T>C
|
XP_011517019.2:p.Pro1400=
|
|