ENST00000651671.1:c.6116A>G
MANE Select
|
ENSP00000498587.1:p.Asn2039Ser
|
|
ENST00000679595.1:c.*1156A>G
|
ENSP00000506241.1:n.*1156A>G
|
|
ENST00000679969.1:n.2712A>G
|
|
|
ENST00000680003.1:n.2448A>G
|
|
|
ENST00000680133.1:c.6002A>G
|
ENSP00000505319.1:p.Asn2001Ser
|
|
ENST00000680218.1:c.5996A>G
|
ENSP00000505339.1:p.Asn1999Ser
|
|
ENST00000680668.1:c.6002A>G
|
ENSP00000506336.1:p.Asn2001Ser
|
|
ENST00000680778.1:c.3713A>G
|
ENSP00000506033.1:p.Asn1238Ser
|
|
ENST00000680924.1:c.*3516A>G
|
ENSP00000506031.1:n.*3516A>G
|
|
ENST00000681135.1:c.*3725A>G
|
ENSP00000506636.1:n.*3725A>G
|
|
ENST00000681298.1:n.4221A>G
|
|
|
ENST00000681454.1:c.*5352A>G
|
ENSP00000505763.1:n.*5352A>G
|
|
ENST00000277541.6:c.6116A>G
|
ENSP00000277541.6:p.Asn2039Ser
|
|
NM_017617.3:c.6116A>G
|
NP_060087.3:p.Asn2039Ser
|
|
XM_011518717.1:c.5417A>G
|
XP_011517019.1:p.Asn1806Ser
|
|
NM_017617.5:c.6116A>G
MANE Select
|
NP_060087.3:p.Asn2039Ser
|
|
XM_011518717.2:c.5393A>G
|
XP_011517019.2:p.Asn1798Ser
|
|