ENST00000547103.7:c.6242A>G
MANE Select
|
ENSP00000447211.2:p.Asn2081Ser
|
|
ENST00000642294.1:c.182A>G
|
ENSP00000493572.1:p.Asn61Ser
|
|
ENST00000646859.1:c.6107A>G
|
ENSP00000496036.1:p.Asn2036Ser
|
|
ENST00000298820.7:c.1527+100A>G
|
|
|
ENST00000458043.6:c.6215A>G
|
ENSP00000400895.2:p.Asn2072Ser
|
|
ENST00000546620.5:n.498A>G
|
|
|
ENST00000547103.5:c.6179A>G
|
ENSP00000447211.1:p.Asn2060Ser
|
|
ENST00000550182.2:c.266A>G
|
ENSP00000449641.1:p.Asn89Ser
|
|
ENST00000551340.5:c.370A>G
|
|
|
NM_173591.3:c.6215A>G
|
NP_775862.3:p.Asn2072Ser
|
|
XM_005268802.2:c.6266A>G
|
XP_005268859.1:p.Asn2089Ser
|
|
XM_011538191.1:c.6266A>G
|
XP_011536493.1:p.Asn2089Ser
|
|
XM_011538192.1:c.6113A>G
|
XP_011536494.1:p.Asn2038Ser
|
|
XM_011538193.1:c.5900A>G
|
XP_011536495.1:p.Asn1967Ser
|
|
XM_005268802.3:c.6266A>G
|
XP_005268859.1:p.Asn2089Ser
|
|
XM_011538192.2:c.6113A>G
|
XP_011536494.1:p.Asn2038Ser
|
|
NM_001368062.1:c.6080A>G
|
NP_001354991.1:p.Asn2027Ser
|
|
NM_001368062.3:c.6107A>G
|
NP_001354991.2:p.Asn2036Ser
|
|
NM_001378609.3:c.6242A>G
MANE Select
|
NP_001365538.2:p.Asn2081Ser
|
|
NM_001378610.3:c.6242A>G
|
NP_001365539.2:p.Asn2081Ser
|
|
NM_173591.7:c.6242A>G
|
NP_775862.4:p.Asn2081Ser
|
|