ENST00000391944.8:c.2120A>C
|
ENSP00000375808.4:p.Asn707Thr
|
|
ENST00000682414.1:c.2120A>C
|
ENSP00000507019.1:p.Asn707Thr
|
|
ENST00000682508.1:n.2149A>C
|
|
|
ENST00000684218.1:c.*1378A>C
|
ENSP00000507804.1:n.*1378A>C
|
|
ENST00000684264.1:n.1676A>C
|
|
|
ENST00000684407.1:c.1997A>C
|
ENSP00000507775.1:p.Asn666Thr
|
|
ENST00000684458.1:c.*606A>C
|
ENSP00000508260.1:n.*606A>C
|
|
ENST00000684468.1:n.1832A>C
|
|
|
ENST00000391945.10:c.2120A>C
MANE Select
|
ENSP00000375809.4:p.Asn707Thr
|
|
ENST00000646507.1:n.2217A>C
|
|
|
ENST00000391941.6:c.2048A>C
|
ENSP00000375805.2:p.Asn683Thr
|
|
ENST00000391942.6:n.1291A>C
|
|
|
ENST00000391944.7:c.1886A>C
|
ENSP00000375808.3:p.Asn629Thr
|
|
ENST00000391945.8:c.2120A>C
|
ENSP00000375809.3:p.Asn707Thr
|
|
ENST00000588652.5:n.2208A>C
|
|
|
NM_000400.3:c.2120A>C , LRG_461t1:c.2120A>C
|
NP_000391.1:p.Asn707Thr
|
|
XM_011526611.1:c.2042A>C
|
XP_011524913.1:p.Asn681Thr
|
|
XM_011526611.2:c.2042A>C
|
XP_011524913.1:p.Asn681Thr
|
|
XM_017026467.1:c.1997A>C
|
XP_016881956.1:p.Asn666Thr
|
|
XR_001753633.2:n.2167A>C
|
|
|
XR_001753634.2:n.2103A>C
|
|
|
NM_000400.4:c.2120A>C
MANE Select
|
NP_000391.1:p.Asn707Thr
|
|