ENST00000645828.1:n.2402A>C
|
|
|
ENST00000651671.1:c.4595A>C
MANE Select
|
ENSP00000498587.1:p.Tyr1532Ser
|
|
ENST00000679595.1:c.4595A>C
|
ENSP00000506241.1:p.Tyr1532Ser
|
|
ENST00000680133.1:c.4481A>C
|
ENSP00000505319.1:p.Tyr1494Ser
|
|
ENST00000680218.1:c.4475A>C
|
ENSP00000505339.1:p.Tyr1492Ser
|
|
ENST00000680668.1:c.4481A>C
|
ENSP00000506336.1:p.Tyr1494Ser
|
|
ENST00000680778.1:c.2192A>C
|
ENSP00000506033.1:p.Tyr731Ser
|
|
ENST00000680924.1:c.*1995A>C
|
ENSP00000506031.1:n.*1995A>C
|
|
ENST00000681135.1:c.*2204A>C
|
ENSP00000506636.1:n.*2204A>C
|
|
ENST00000681298.1:n.1408A>C
|
|
|
ENST00000681454.1:c.*3831A>C
|
ENSP00000505763.1:n.*3831A>C
|
|
ENST00000277541.6:c.4595A>C
|
ENSP00000277541.6:p.Tyr1532Ser
|
|
NM_017617.3:c.4595A>C
|
NP_060087.3:p.Tyr1532Ser
|
|
XM_011518717.1:c.3896A>C
|
XP_011517019.1:p.Tyr1299Ser
|
|
NM_017617.5:c.4595A>C
MANE Select
|
NP_060087.3:p.Tyr1532Ser
|
|
XM_011518717.2:c.3872A>C
|
XP_011517019.2:p.Tyr1291Ser
|
|