ENST00000703783.1:n.653A>C
|
|
|
ENST00000703785.1:n.734A>C
|
|
|
ENST00000262464.9:c.3869A>C
MANE Select
|
ENSP00000262464.4:p.Asn1290Thr
|
|
ENST00000262464.8:c.3869A>C
|
ENSP00000262464.4:p.Asn1290Thr
|
|
ENST00000507835.5:c.419A>C
|
ENSP00000426839.1:p.Asn140Thr
|
|
ENST00000508053.5:c.3869A>C
|
ENSP00000424571.1:p.Asn1290Thr
|
|
ENST00000508989.5:c.3770A>C
|
ENSP00000425596.1:p.Asn1257Thr
|
|
ENST00000619499.4:c.3866A>C
|
ENSP00000482132.1:p.Asn1289Thr
|
|
NM_001999.3:c.3869A>C
|
NP_001990.2:p.Asn1290Thr
|
|
XM_017009228.2:c.3716A>C
|
XP_016864717.1:p.Asn1239Thr
|
|
NM_001999.4:c.3869A>C
MANE Select
|
NP_001990.2:p.Asn1290Thr
|
|