|
ENST00000257863.9:c.1287T>G
MANE Select
|
ENSP00000257863.3:p.Pro429=
|
|
|
ENST00000257863.8:c.1287T>G
|
ENSP00000257863.3:p.Pro429=
|
|
|
ENST00000379791.7:c.1140+352T>G
|
ENSP00000369117.3:n.1140+352T>G
|
|
|
ENST00000550311.5:c.1287T>G
|
ENSP00000446661.1:p.Pro429=
|
|
|
ENST00000550839.1:c.378T>G
|
ENSP00000455338.1:p.Pro126=
|
|
|
ENST00000552233.5:n.875T>G
|
|
|
|
NM_001164690.1:c.1287T>G
|
NP_001158162.1:p.Pro429=
|
|
|
NM_001164691.1:c.1140+352T>G
|
NP_001158163.1:n.1140+352T>G
|
|
|
NM_020547.2:c.1287T>G
|
NP_065434.1:p.Pro429=
|
|
|
XM_011538173.1:c.1347T>G
|
XP_011536475.1:p.Pro449=
|
|
|
XM_011538174.1:c.1344T>G
|
XP_011536476.1:p.Pro448=
|
|
|
XM_011538175.1:c.1329T>G
|
XP_011536477.1:p.Pro443=
|
|
|
XM_011538176.1:c.1290T>G
|
XP_011536478.1:p.Pro430=
|
|
|
XM_011538177.1:c.1269T>G
|
XP_011536479.1:p.Pro423=
|
|
|
XM_011538178.1:c.1128T>G
|
XP_011536480.1:p.Pro376=
|
|
|
XM_011538179.1:c.1200+352T>G
|
XP_011536481.1:n.1200+352T>G
|
|
|
XM_011538180.1:c.1014T>G
|
XP_011536482.1:p.Pro338=
|
|
|
XM_011538181.1:c.1011T>G
|
XP_011536483.1:p.Pro337=
|
|
|
XM_011538182.1:c.936T>G
|
XP_011536484.1:p.Pro312=
|
|
|
XM_011538183.1:c.1201-169T>G
|
XP_011536485.1:n.1201-169T>G
|
|
|
XM_011538184.1:c.1220+332T>G
|
XP_011536486.1:n.1220+332T>G
|
|
|
XM_011538185.1:c.856-1200T>G
|
XP_011536487.1:n.856-1200T>G
|
|
|
XM_011538186.1:c.462T>G
|
XP_011536488.1:p.Pro154=
|
|
|
NM_001164690.2:c.1287T>G
|
NP_001158162.1:p.Pro429=
|
|
|
NM_001164691.2:c.1140+352T>G
|
NP_001158163.1:n.1140+352T>G
|
|
|
NM_020547.3:c.1287T>G
MANE Select
|
NP_065434.1:p.Pro429=
|
|
|
XM_011538183.2:c.1201-169T>G
|
XP_011536485.1:n.1201-169T>G
|
|
|
XM_011538184.2:c.1220+332T>G
|
XP_011536486.1:n.1220+332T>G
|
|
|
XM_011538186.3:c.462T>G
|
XP_011536488.1:p.Pro154=
|
|
|
XM_017019179.2:c.1347T>G
|
XP_016874668.1:p.Pro449=
|
|
|
XM_024448938.1:c.1143+352T>G
|
XP_024304706.1:n.1143+352T>G
|
|
|
XR_002957309.1:n.1255T>G
|
|
|
|
XR_002957310.1:n.1109-169T>G
|
|
|
|
XR_002957311.1:n.1255T>G
|
|
|
|
XR_002957312.1:n.1108+352T>G
|
|
|
