ENST00000299314.12:c.2096A>C
MANE Select
|
ENSP00000299314.7:p.Asn699Thr
|
|
ENST00000299314.11:c.2096A>C
|
ENSP00000299314.7:p.Asn699Thr
|
|
NM_024312.4:c.2096A>C
|
NP_077288.2:p.Asn699Thr
|
|
XM_006719593.2:c.2096A>C
|
XP_006719656.1:p.Asn699Thr
|
|
XM_011538731.1:c.2015A>C
|
XP_011537033.1:p.Asn672Thr
|
|
XM_006719593.3:c.2096A>C
|
XP_006719656.1:p.Asn699Thr
|
|
XM_011538731.2:c.2015A>C
|
XP_011537033.1:p.Asn672Thr
|
|
XM_017019961.1:c.1880A>C
|
XP_016875450.1:p.Asn627Thr
|
|
XM_017019962.2:c.869A>C
|
XP_016875451.1:p.Asn290Thr
|
|
NM_024312.5:c.2096A>C
MANE Select
|
NP_077288.2:p.Asn699Thr
|
|