ENST00000338508.9:c.3227T>G
|
ENSP00000345193.7:p.Met1076Arg
|
|
ENST00000412252.6:c.772T>G
|
ENSP00000414876.2:p.Ter258Gly
|
|
ENST00000601538.6:c.4994T>G
MANE Select
|
ENSP00000469689.2:p.Met1665Arg
|
|
ENST00000654939.1:c.2503T>G
|
|
|
ENST00000656230.1:c.3857T>G
|
ENSP00000499561.1:p.Met1286Arg
|
|
ENST00000659264.1:c.3284T>G
|
ENSP00000499270.1:p.Met1095Arg
|
|
ENST00000338508.8:c.3230T>G
|
ENSP00000345193.6:p.Met1077Arg
|
|
ENST00000357171.7:c.733T>G
|
ENSP00000349694.4:p.Ter245Gly
|
|
ENST00000409161.5:c.3206T>G
|
ENSP00000386491.1:p.Met1069Arg
|
|
ENST00000412252.5:c.770T>G
|
|
|
ENST00000423696.6:c.3857T>G
|
ENSP00000394536.2:p.Met1286Arg
|
|
ENST00000424924.5:c.2831T>G
|
ENSP00000402944.1:p.Met944Arg
|
|
ENST00000449833.6:c.3230T>G
|
ENSP00000399423.3:p.Met1077Arg
|
|
ENST00000601538.5:c.4994T>G
|
ENSP00000469689.2:p.Met1665Arg
|
|
ENST00000606715.3:n.1746T>G
|
|
|
NM_012309.4:c.4994T>G
|
NP_036441.2:p.Met1665Arg
|
|
NM_133266.4:c.3230T>G
|
NP_573573.2:p.Met1077Arg
|
|
NR_110766.1:n.848T>G
|
|
|
XM_005277930.2:c.4994T>G
|
XP_005277987.1:p.Met1665Arg
|
|
XM_005277932.2:c.3857T>G
|
XP_005277989.1:p.Met1286Arg
|
|
XM_006718478.2:c.4964T>G
|
XP_006718541.1:p.Met1655Arg
|
|
XM_011544854.1:c.5006T>G
|
XP_011543156.1:p.Met1669Arg
|
|
XM_011544855.1:c.4985T>G
|
XP_011543157.1:p.Met1662Arg
|
|
XM_011544856.1:c.4979T>G
|
XP_011543158.1:p.Met1660Arg
|
|
XM_011544857.1:c.4958T>G
|
XP_011543159.1:p.Met1653Arg
|
|
XM_011544859.1:c.3869T>G
|
XP_011543161.1:p.Met1290Arg
|
|
XM_005277932.3:c.3857T>G
|
XP_005277989.1:p.Met1286Arg
|
|
XM_017017387.1:c.4994T>G
|
XP_016872876.1:p.Met1665Arg
|
|
XM_017017388.1:c.4994T>G
|
XP_016872877.1:p.Met1665Arg
|
|
XM_017017389.1:c.4967T>G
|
XP_016872878.1:p.Met1656Arg
|
|
XM_017017390.1:c.3284T>G
|
XP_016872879.1:p.Met1095Arg
|
|
NM_133266.5:c.3230T>G
|
NP_573573.2:p.Met1077Arg
|
|
NR_110766.2:n.849T>G
|
|
|
NM_001379226.1:c.3857T>G
|
NP_001366155.1:p.Met1286Arg
|
|
NM_012309.5:c.4994T>G
MANE Select
|
NP_036441.2:p.Met1665Arg
|
|