ENST00000338508.9:c.3363T>G
|
ENSP00000345193.7:p.Pro1121=
|
|
ENST00000412252.6:c.908T>G
|
ENSP00000414876.2:n.908T>G
|
|
ENST00000601538.6:c.5130T>G
MANE Select
|
ENSP00000469689.2:p.Pro1710=
|
|
ENST00000654939.1:c.2639T>G
|
|
|
ENST00000656230.1:c.3993T>G
|
ENSP00000499561.1:p.Pro1331=
|
|
ENST00000659264.1:c.3420T>G
|
ENSP00000499270.1:p.Pro1140=
|
|
ENST00000338508.8:c.3366T>G
|
ENSP00000345193.6:p.Pro1122=
|
|
ENST00000357171.7:c.*134T>G
|
ENSP00000349694.4:n.*134T>G
|
|
ENST00000409161.5:c.3342T>G
|
ENSP00000386491.1:p.Pro1114=
|
|
ENST00000412252.5:c.906T>G
|
|
|
ENST00000423696.6:c.3993T>G
|
ENSP00000394536.2:p.Pro1331=
|
|
ENST00000424924.5:c.2967T>G
|
ENSP00000402944.1:p.Pro989=
|
|
ENST00000449833.6:c.3366T>G
|
ENSP00000399423.3:p.Pro1122=
|
|
ENST00000601538.5:c.5130T>G
|
ENSP00000469689.2:p.Pro1710=
|
|
ENST00000606715.3:n.1882T>G
|
|
|
NM_012309.4:c.5130T>G
|
NP_036441.2:p.Pro1710=
|
|
NM_133266.4:c.3366T>G
|
NP_573573.2:p.Pro1122=
|
|
NR_110766.1:n.984T>G
|
|
|
XM_005277930.2:c.5130T>G
|
XP_005277987.1:p.Pro1710=
|
|
XM_005277932.2:c.3993T>G
|
XP_005277989.1:p.Pro1331=
|
|
XM_006718478.2:c.5100T>G
|
XP_006718541.1:p.Pro1700=
|
|
XM_011544854.1:c.5142T>G
|
XP_011543156.1:p.Pro1714=
|
|
XM_011544855.1:c.5121T>G
|
XP_011543157.1:p.Pro1707=
|
|
XM_011544856.1:c.5115T>G
|
XP_011543158.1:p.Pro1705=
|
|
XM_011544857.1:c.5094T>G
|
XP_011543159.1:p.Pro1698=
|
|
XM_011544859.1:c.4005T>G
|
XP_011543161.1:p.Pro1335=
|
|
XM_005277932.3:c.3993T>G
|
XP_005277989.1:p.Pro1331=
|
|
XM_017017387.1:c.5130T>G
|
XP_016872876.1:p.Pro1710=
|
|
XM_017017388.1:c.5130T>G
|
XP_016872877.1:p.Pro1710=
|
|
XM_017017389.1:c.5103T>G
|
XP_016872878.1:p.Pro1701=
|
|
XM_017017390.1:c.3420T>G
|
XP_016872879.1:p.Pro1140=
|
|
NM_133266.5:c.3366T>G
|
NP_573573.2:p.Pro1122=
|
|
NR_110766.2:n.985T>G
|
|
|
NM_001379226.1:c.3993T>G
|
NP_001366155.1:p.Pro1331=
|
|
NM_012309.5:c.5130T>G
MANE Select
|
NP_036441.2:p.Pro1710=
|
|