|
ENST00000338508.9:c.3246A>C
|
ENSP00000345193.7:p.Thr1082=
|
|
|
ENST00000412252.6:c.791A>C
|
ENSP00000414876.2:n.791A>C
|
|
|
ENST00000601538.6:c.5013A>C
MANE Select
|
ENSP00000469689.2:p.Thr1671=
|
|
|
ENST00000654939.1:c.2522A>C
|
|
|
|
ENST00000656230.1:c.3876A>C
|
ENSP00000499561.1:p.Thr1292=
|
|
|
ENST00000659264.1:c.3303A>C
|
ENSP00000499270.1:p.Thr1101=
|
|
|
ENST00000338508.8:c.3249A>C
|
ENSP00000345193.6:p.Thr1083=
|
|
|
ENST00000357171.7:c.*17A>C
|
ENSP00000349694.4:n.*17A>C
|
|
|
ENST00000409161.5:c.3225A>C
|
ENSP00000386491.1:p.Thr1075=
|
|
|
ENST00000412252.5:c.789A>C
|
|
|
|
ENST00000423696.6:c.3876A>C
|
ENSP00000394536.2:p.Thr1292=
|
|
|
ENST00000424924.5:c.2850A>C
|
ENSP00000402944.1:p.Thr950=
|
|
|
ENST00000449833.6:c.3249A>C
|
ENSP00000399423.3:p.Thr1083=
|
|
|
ENST00000601538.5:c.5013A>C
|
ENSP00000469689.2:p.Thr1671=
|
|
|
ENST00000606715.3:n.1765A>C
|
|
|
|
NM_012309.4:c.5013A>C
|
NP_036441.2:p.Thr1671=
|
|
|
NM_133266.4:c.3249A>C
|
NP_573573.2:p.Thr1083=
|
|
|
NR_110766.1:n.867A>C
|
|
|
|
XM_005277930.2:c.5013A>C
|
XP_005277987.1:p.Thr1671=
|
|
|
XM_005277932.2:c.3876A>C
|
XP_005277989.1:p.Thr1292=
|
|
|
XM_006718478.2:c.4983A>C
|
XP_006718541.1:p.Thr1661=
|
|
|
XM_011544854.1:c.5025A>C
|
XP_011543156.1:p.Thr1675=
|
|
|
XM_011544855.1:c.5004A>C
|
XP_011543157.1:p.Thr1668=
|
|
|
XM_011544856.1:c.4998A>C
|
XP_011543158.1:p.Thr1666=
|
|
|
XM_011544857.1:c.4977A>C
|
XP_011543159.1:p.Thr1659=
|
|
|
XM_011544859.1:c.3888A>C
|
XP_011543161.1:p.Thr1296=
|
|
|
XM_005277932.3:c.3876A>C
|
XP_005277989.1:p.Thr1292=
|
|
|
XM_017017387.1:c.5013A>C
|
XP_016872876.1:p.Thr1671=
|
|
|
XM_017017388.1:c.5013A>C
|
XP_016872877.1:p.Thr1671=
|
|
|
XM_017017389.1:c.4986A>C
|
XP_016872878.1:p.Thr1662=
|
|
|
XM_017017390.1:c.3303A>C
|
XP_016872879.1:p.Thr1101=
|
|
|
NM_133266.5:c.3249A>C
|
NP_573573.2:p.Thr1083=
|
|
|
NR_110766.2:n.868A>C
|
|
|
|
NM_001379226.1:c.3876A>C
|
NP_001366155.1:p.Thr1292=
|
|
|
NM_012309.5:c.5013A>C
MANE Select
|
NP_036441.2:p.Thr1671=
|
|
