ENST00000695850.1:n.1456T>C
|
|
|
ENST00000695852.1:n.387T>C
|
|
|
ENST00000695853.1:c.*1339T>C
|
ENSP00000512218.1:n.*1339T>C
|
|
ENST00000423902.7:c.8280T>C
MANE Select
|
ENSP00000392028.1:p.Asn2760=
|
|
ENST00000423902.6:c.8280T>C
|
ENSP00000392028.1:p.Asn2760=
|
|
ENST00000524602.5:c.2133T>C
|
ENSP00000437061.1:p.Asn711=
|
|
ENST00000528280.1:n.326T>C
|
|
|
NM_001316690.1:c.2133T>C
|
NP_001303619.1:p.Asn711=
|
|
NM_017780.3:c.8280T>C
|
NP_060250.2:p.Asn2760=
|
|
XM_011517553.1:c.8370T>C
|
XP_011515855.1:p.Asn2790=
|
|
XM_011517554.1:c.8370T>C
|
XP_011515856.1:p.Asn2790=
|
|
XM_011517555.1:c.8367T>C
|
XP_011515857.1:p.Asn2789=
|
|
XM_011517556.1:c.8148T>C
|
XP_011515858.1:p.Asn2716=
|
|
XM_011517557.1:c.6357T>C
|
XP_011515859.1:p.Asn2119=
|
|
XM_011517558.1:c.5907T>C
|
XP_011515860.1:p.Asn1969=
|
|
XM_011517559.1:c.5115T>C
|
XP_011515861.1:p.Asn1705=
|
|
XM_011517553.2:c.8370T>C
|
XP_011515855.1:p.Asn2790=
|
|
XM_011517554.3:c.8370T>C
|
XP_011515856.1:p.Asn2790=
|
|
XM_011517555.2:c.8367T>C
|
XP_011515857.1:p.Asn2789=
|
|
XM_017013612.1:c.8370T>C
|
XP_016869101.1:p.Asn2790=
|
|
XM_017013613.1:c.8277T>C
|
XP_016869102.1:p.Asn2759=
|
|
NM_017780.4:c.8280T>C
MANE Select
|
NP_060250.2:p.Asn2760=
|
|