|
ENST00000269571.10:c.3347C>G
MANE Select
|
ENSP00000269571.4:p.Pro1116Arg
|
|
|
ENST00000269571.9:c.3347C>G
|
ENSP00000269571.4:p.Pro1116Arg
|
|
|
ENST00000406381.6:c.3257C>G
|
ENSP00000385185.2:p.Pro1086Arg
|
|
|
ENST00000445658.6:c.2519C>G
|
ENSP00000404047.2:p.Pro840Arg
|
|
|
ENST00000541774.5:c.3302C>G
|
ENSP00000446466.1:p.Pro1101Arg
|
|
|
ENST00000578373.5:c.*3137C>G
|
ENSP00000463427.1:n.*3137C>G
|
|
|
ENST00000584450.5:c.3160-207C>G
|
ENSP00000463714.1:n.3160-207C>G
|
|
|
ENST00000584601.5:c.3257C>G
|
ENSP00000462438.1:p.Pro1086Arg
|
|
|
NM_001005862.2:c.3257C>G , LRG_724t1:c.3257C>G
|
NP_001005862.1:p.Pro1086Arg
|
|
|
NM_001289936.1:c.3302C>G , LRG_724t4:c.3302C>G
|
NP_001276865.1:p.Pro1101Arg
|
|
|
NM_001289937.1:c.3160-207C>G
|
NP_001276866.1:n.3160-207C>G
|
|
|
NM_004448.3:c.3347C>G , LRG_724t2:c.3347C>G
|
NP_004439.2:p.Pro1116Arg
|
|
|
NR_110535.1:n.3671C>G
|
|
|
|
XM_024450641.1:c.3485C>G
|
XP_024306409.1:p.Pro1162Arg
|
|
|
XM_024450642.1:c.3440C>G
|
XP_024306410.1:p.Pro1147Arg
|
|
|
XM_024450643.1:c.3395C>G
|
XP_024306411.1:p.Pro1132Arg
|
|
|
NM_001005862.3:c.3257C>G
|
NP_001005862.1:p.Pro1086Arg
|
|
|
NM_001289936.2:c.3302C>G
|
NP_001276865.1:p.Pro1101Arg
|
|
|
NM_001289937.2:c.3160-207C>G
|
NP_001276866.1:n.3160-207C>G
|
|
|
NM_001382782.1:c.3257C>G
|
NP_001369711.1:p.Pro1086Arg
|
|
|
NM_001382783.1:c.3257C>G
|
NP_001369712.1:p.Pro1086Arg
|
|
|
NM_001382784.1:c.3464C>G
|
NP_001369713.1:p.Pro1155Arg
|
|
|
NM_001382785.1:c.3449C>G
|
NP_001369714.1:p.Pro1150Arg
|
|
|
NM_001382786.1:c.3428C>G
|
NP_001369715.1:p.Pro1143Arg
|
|
|
NM_001382787.1:c.3422C>G
|
NP_001369716.1:p.Pro1141Arg
|
|
|
NM_001382788.1:c.3377C>G
|
NP_001369717.1:p.Pro1126Arg
|
|
|
NM_001382789.1:c.3368C>G
|
NP_001369718.1:p.Pro1123Arg
|
|
|
NM_001382790.1:c.3344C>G
|
NP_001369719.1:p.Pro1115Arg
|
|
|
NM_001382791.1:c.3338C>G
|
NP_001369720.1:p.Pro1113Arg
|
|
|
NM_001382792.1:c.3311C>G
|
NP_001369721.1:p.Pro1104Arg
|
|
|
NM_001382793.1:c.3305C>G
|
NP_001369722.1:p.Pro1102Arg
|
|
|
NM_001382794.1:c.3305C>G
|
NP_001369723.1:p.Pro1102Arg
|
|
|
NM_001382795.1:c.3299C>G
|
NP_001369724.1:p.Pro1100Arg
|
|
|
NM_001382796.1:c.3260C>G
|
NP_001369725.1:p.Pro1087Arg
|
|
|
NM_001382797.1:c.3248C>G
|
NP_001369726.1:p.Pro1083Arg
|
|
|
NM_001382798.1:c.3191C>G
|
NP_001369727.1:p.Pro1064Arg
|
|
|
NM_001382799.1:c.3167C>G
|
NP_001369728.1:p.Pro1056Arg
|
|
|
NM_001382800.1:c.3161C>G
|
NP_001369729.1:p.Pro1054Arg
|
|
|
NM_001382801.1:c.3143C>G
|
NP_001369730.1:p.Pro1048Arg
|
|
|
NM_001382802.1:c.3089C>G
|
NP_001369731.1:p.Pro1030Arg
|
|
|
NM_001382803.1:c.3118-207C>G
|
NP_001369732.1:n.3118-207C>G
|
|
|
NM_001382804.1:c.2519C>G
|
NP_001369733.1:p.Pro840Arg
|
|
|
NM_001382805.1:c.2396C>G
|
NP_001369734.1:p.Pro799Arg
|
|
|
NM_001382806.1:c.2309C>G
|
NP_001369735.1:p.Pro770Arg
|
|
|
NM_004448.4:c.3347C>G
MANE Select
|
NP_004439.2:p.Pro1116Arg
|
|
|
NR_110535.2:n.3585C>G
|
|
|
