|
ENST00000415928.6:c.1048A>G
|
ENSP00000388838.2:p.Met350Val
|
|
|
ENST00000435065.7:c.1279A>G
|
ENSP00000402760.2:p.Met427Val
|
|
|
ENST00000448810.6:c.*59A>G
|
ENSP00000401860.2:n.*59A>G
|
|
|
ENST00000685543.1:n.1348A>G
|
|
|
|
ENST00000686757.1:c.*371A>G
|
ENSP00000510721.1:n.*371A>G
|
|
|
ENST00000687740.1:n.3892A>G
|
|
|
|
ENST00000688151.1:n.2517A>G
|
|
|
|
ENST00000689271.1:c.1054A>G
|
ENSP00000510797.1:p.Met352Val
|
|
|
ENST00000690900.1:c.*371A>G
|
ENSP00000510703.1:n.*371A>G
|
|
|
ENST00000692212.1:n.2819A>G
|
|
|
|
ENST00000692355.1:c.460A>G
|
|
|
|
ENST00000692413.1:c.1189A>G
|
ENSP00000509374.1:p.Met397Val
|
|
|
ENST00000692825.1:c.1275A>G
|
ENSP00000509447.1:n.1275A>G
|
|
|
ENST00000693308.1:c.1255A>G
|
ENSP00000509770.1:p.Met419Val
|
|
|
ENST00000693763.1:n.2367A>G
|
|
|
|
ENST00000245407.8:c.1207A>G
MANE Select
|
ENSP00000245407.3:p.Met403Val
|
|
|
ENST00000245407.7:c.1207A>G
|
ENSP00000245407.3:p.Met403Val
|
|
|
ENST00000435065.6:c.1279A>G
|
ENSP00000402760.2:p.Met427Val
|
|
|
ENST00000447841.5:c.112-1589A>G
|
|
|
|
ENST00000448810.5:c.469A>G
|
|
|
|
ENST00000461013.5:n.8629A>G
|
|
|
|
ENST00000475308.1:n.1885A>G
|
|
|
|
ENST00000479605.5:n.310A>G
|
|
|
|
NM_001308122.1:c.1279A>G
|
NP_001295051.1:p.Met427Val
|
|
|
NM_003060.3:c.1207A>G
|
NP_003051.1:p.Met403Val
|
|
|
XM_011543590.1:c.589A>G
|
XP_011541892.1:p.Met197Val
|
|
|
XR_427718.1:n.1567A>G
|
|
|
|
XR_948290.1:n.1394-1589A>G
|
|
|
|
XR_948291.1:n.1561A>G
|
|
|
|
XM_011543590.2:c.589A>G
|
XP_011541892.1:p.Met197Val
|
|
|
XM_017009778.2:c.679A>G
|
XP_016865267.1:p.Met227Val
|
|
|
XR_001742215.1:n.1462A>G
|
|
|
|
XR_001742216.1:n.1481A>G
|
|
|
|
XR_427718.2:n.1567A>G
|
|
|
|
XR_948290.2:n.1394-1589A>G
|
|
|
|
XR_948291.2:n.1561A>G
|
|
|
|
NM_003060.4:c.1207A>G
MANE Select
|
NP_003051.1:p.Met403Val
|
|
|
NM_001308122.2:c.1279A>G
|
NP_001295051.1:p.Met427Val
|
|
