ENST00000338508.9:c.3440C>T
|
ENSP00000345193.7:p.Ala1147Val
|
|
ENST00000412252.6:c.985C>T
|
ENSP00000414876.2:n.985C>T
|
|
ENST00000601538.6:c.5207C>T
MANE Select
|
ENSP00000469689.2:p.Ala1736Val
|
|
ENST00000654939.1:c.2716C>T
|
|
|
ENST00000656230.1:c.4070C>T
|
ENSP00000499561.1:p.Ala1357Val
|
|
ENST00000659264.1:c.3497C>T
|
ENSP00000499270.1:p.Ala1166Val
|
|
ENST00000338508.8:c.3443C>T
|
ENSP00000345193.6:p.Ala1148Val
|
|
ENST00000357171.7:c.*211C>T
|
ENSP00000349694.4:n.*211C>T
|
|
ENST00000409161.5:c.3419C>T
|
ENSP00000386491.1:p.Ala1140Val
|
|
ENST00000412252.5:c.983C>T
|
|
|
ENST00000423696.6:c.4070C>T
|
ENSP00000394536.2:p.Ala1357Val
|
|
ENST00000424924.5:c.3044C>T
|
ENSP00000402944.1:p.Ala1015Val
|
|
ENST00000449833.6:c.3443C>T
|
ENSP00000399423.3:p.Ala1148Val
|
|
ENST00000601538.5:c.5207C>T
|
ENSP00000469689.2:p.Ala1736Val
|
|
ENST00000606715.3:n.1959C>T
|
|
|
NM_012309.4:c.5207C>T
|
NP_036441.2:p.Ala1736Val
|
|
NM_133266.4:c.3443C>T
|
NP_573573.2:p.Ala1148Val
|
|
NR_110766.1:n.1061C>T
|
|
|
XM_005277930.2:c.5207C>T
|
XP_005277987.1:p.Ala1736Val
|
|
XM_005277932.2:c.4070C>T
|
XP_005277989.1:p.Ala1357Val
|
|
XM_006718478.2:c.5177C>T
|
XP_006718541.1:p.Ala1726Val
|
|
XM_011544854.1:c.5219C>T
|
XP_011543156.1:p.Ala1740Val
|
|
XM_011544855.1:c.5198C>T
|
XP_011543157.1:p.Ala1733Val
|
|
XM_011544856.1:c.5192C>T
|
XP_011543158.1:p.Ala1731Val
|
|
XM_011544857.1:c.5171C>T
|
XP_011543159.1:p.Ala1724Val
|
|
XM_011544859.1:c.4082C>T
|
XP_011543161.1:p.Ala1361Val
|
|
XM_005277932.3:c.4070C>T
|
XP_005277989.1:p.Ala1357Val
|
|
XM_017017387.1:c.5207C>T
|
XP_016872876.1:p.Ala1736Val
|
|
XM_017017388.1:c.5207C>T
|
XP_016872877.1:p.Ala1736Val
|
|
XM_017017389.1:c.5180C>T
|
XP_016872878.1:p.Ala1727Val
|
|
XM_017017390.1:c.3497C>T
|
XP_016872879.1:p.Ala1166Val
|
|
NM_133266.5:c.3443C>T
|
NP_573573.2:p.Ala1148Val
|
|
NR_110766.2:n.1062C>T
|
|
|
NM_001379226.1:c.4070C>T
|
NP_001366155.1:p.Ala1357Val
|
|
NM_012309.5:c.5207C>T
MANE Select
|
NP_036441.2:p.Ala1736Val
|
|