ENST00000338508.9:c.3245C>G
|
ENSP00000345193.7:p.Thr1082Arg
|
|
ENST00000412252.6:c.790C>G
|
ENSP00000414876.2:n.790C>G
|
|
ENST00000601538.6:c.5012C>G
MANE Select
|
ENSP00000469689.2:p.Thr1671Arg
|
|
ENST00000654939.1:c.2521C>G
|
|
|
ENST00000656230.1:c.3875C>G
|
ENSP00000499561.1:p.Thr1292Arg
|
|
ENST00000659264.1:c.3302C>G
|
ENSP00000499270.1:p.Thr1101Arg
|
|
ENST00000338508.8:c.3248C>G
|
ENSP00000345193.6:p.Thr1083Arg
|
|
ENST00000357171.7:c.*16C>G
|
ENSP00000349694.4:n.*16C>G
|
|
ENST00000409161.5:c.3224C>G
|
ENSP00000386491.1:p.Thr1075Arg
|
|
ENST00000412252.5:c.788C>G
|
|
|
ENST00000423696.6:c.3875C>G
|
ENSP00000394536.2:p.Thr1292Arg
|
|
ENST00000424924.5:c.2849C>G
|
ENSP00000402944.1:p.Thr950Arg
|
|
ENST00000449833.6:c.3248C>G
|
ENSP00000399423.3:p.Thr1083Arg
|
|
ENST00000601538.5:c.5012C>G
|
ENSP00000469689.2:p.Thr1671Arg
|
|
ENST00000606715.3:n.1764C>G
|
|
|
NM_012309.4:c.5012C>G
|
NP_036441.2:p.Thr1671Arg
|
|
NM_133266.4:c.3248C>G
|
NP_573573.2:p.Thr1083Arg
|
|
NR_110766.1:n.866C>G
|
|
|
XM_005277930.2:c.5012C>G
|
XP_005277987.1:p.Thr1671Arg
|
|
XM_005277932.2:c.3875C>G
|
XP_005277989.1:p.Thr1292Arg
|
|
XM_006718478.2:c.4982C>G
|
XP_006718541.1:p.Thr1661Arg
|
|
XM_011544854.1:c.5024C>G
|
XP_011543156.1:p.Thr1675Arg
|
|
XM_011544855.1:c.5003C>G
|
XP_011543157.1:p.Thr1668Arg
|
|
XM_011544856.1:c.4997C>G
|
XP_011543158.1:p.Thr1666Arg
|
|
XM_011544857.1:c.4976C>G
|
XP_011543159.1:p.Thr1659Arg
|
|
XM_011544859.1:c.3887C>G
|
XP_011543161.1:p.Thr1296Arg
|
|
XM_005277932.3:c.3875C>G
|
XP_005277989.1:p.Thr1292Arg
|
|
XM_017017387.1:c.5012C>G
|
XP_016872876.1:p.Thr1671Arg
|
|
XM_017017388.1:c.5012C>G
|
XP_016872877.1:p.Thr1671Arg
|
|
XM_017017389.1:c.4985C>G
|
XP_016872878.1:p.Thr1662Arg
|
|
XM_017017390.1:c.3302C>G
|
XP_016872879.1:p.Thr1101Arg
|
|
NM_133266.5:c.3248C>G
|
NP_573573.2:p.Thr1083Arg
|
|
NR_110766.2:n.867C>G
|
|
|
NM_001379226.1:c.3875C>G
|
NP_001366155.1:p.Thr1292Arg
|
|
NM_012309.5:c.5012C>G
MANE Select
|
NP_036441.2:p.Thr1671Arg
|
|