ENST00000366548.8:c.2498A>C
MANE Select
|
ENSP00000355506.3:p.Asn833Thr
|
|
ENST00000348581.9:c.2498A>C
|
ENSP00000311873.5:p.Asn833Thr
|
|
ENST00000366548.7:c.2498A>C
|
ENSP00000355506.3:p.Asn833Thr
|
|
ENST00000518483.5:c.*84A>C
|
ENSP00000430251.1:n.*84A>C
|
|
ENST00000518741.1:n.152-2967A>C
|
|
|
ENST00000521202.2:c.591A>C
|
|
|
NM_003686.4:c.*84A>C
|
NP_003677.4:n.*84A>C
|
|
NM_006027.4:c.2498A>C
|
NP_006018.4:p.Asn833Thr
|
|
NM_130398.3:c.2498A>C
|
NP_569082.2:p.Asn833Thr
|
|
XM_005273350.2:c.2495A>C
|
XP_005273407.1:p.Asn832Thr
|
|
XM_006711840.1:c.2498A>C
|
XP_006711903.1:p.Asn833Thr
|
|
XM_011544321.1:c.2498A>C
|
XP_011542623.1:p.Asn833Thr
|
|
XM_011544322.1:c.2498A>C
|
XP_011542624.1:p.Asn833Thr
|
|
XM_011544323.1:c.2495A>C
|
XP_011542625.1:p.Asn832Thr
|
|
XM_011544324.1:c.2378A>C
|
XP_011542626.1:p.Asn793Thr
|
|
XM_011544325.1:c.1535A>C
|
XP_011542627.1:p.Asn512Thr
|
|
XR_949162.1:n.2990+4050A>C
|
|
|
NM_001319224.1:c.2495A>C
|
NP_001306153.1:p.Asn832Thr
|
|
XM_006711840.2:c.2498A>C
|
XP_006711903.1:p.Asn833Thr
|
|
XM_011544321.2:c.2498A>C
|
XP_011542623.1:p.Asn833Thr
|
|
XM_011544323.2:c.2495A>C
|
XP_011542625.1:p.Asn832Thr
|
|
XM_011544324.2:c.2378A>C
|
XP_011542626.1:p.Asn793Thr
|
|
XM_011544325.2:c.1535A>C
|
XP_011542627.1:p.Asn512Thr
|
|
XM_017002793.2:c.2378A>C
|
XP_016858282.1:p.Asn793Thr
|
|
NM_130398.4:c.2498A>C
MANE Select
|
NP_569082.2:p.Asn833Thr
|
|
NM_001319224.2:c.2495A>C
|
NP_001306153.1:p.Asn832Thr
|
|