|
ENST00000269571.10:c.3194C>G
MANE Select
|
ENSP00000269571.4:p.Pro1065Arg
|
|
|
ENST00000269571.9:c.3194C>G
|
ENSP00000269571.4:p.Pro1065Arg
|
|
|
ENST00000406381.6:c.3104C>G
|
ENSP00000385185.2:p.Pro1035Arg
|
|
|
ENST00000445658.6:c.2366C>G
|
ENSP00000404047.2:p.Pro789Arg
|
|
|
ENST00000541774.5:c.3149C>G
|
ENSP00000446466.1:p.Pro1050Arg
|
|
|
ENST00000578373.5:c.*2984C>G
|
ENSP00000463427.1:n.*2984C>G
|
|
|
ENST00000584450.5:c.3159+326C>G
|
ENSP00000463714.1:n.3159+326C>G
|
|
|
ENST00000584601.5:c.3104C>G
|
ENSP00000462438.1:p.Pro1035Arg
|
|
|
NM_001005862.2:c.3104C>G , LRG_724t1:c.3104C>G
|
NP_001005862.1:p.Pro1035Arg
|
|
|
NM_001289936.1:c.3149C>G , LRG_724t4:c.3149C>G
|
NP_001276865.1:p.Pro1050Arg
|
|
|
NM_001289937.1:c.3159+326C>G
|
NP_001276866.1:n.3159+326C>G
|
|
|
NM_004448.3:c.3194C>G , LRG_724t2:c.3194C>G
|
NP_004439.2:p.Pro1065Arg
|
|
|
NR_110535.1:n.3518C>G
|
|
|
|
XM_024450641.1:c.3332C>G
|
XP_024306409.1:p.Pro1111Arg
|
|
|
XM_024450642.1:c.3287C>G
|
XP_024306410.1:p.Pro1096Arg
|
|
|
XM_024450643.1:c.3242C>G
|
XP_024306411.1:p.Pro1081Arg
|
|
|
NM_001005862.3:c.3104C>G
|
NP_001005862.1:p.Pro1035Arg
|
|
|
NM_001289936.2:c.3149C>G
|
NP_001276865.1:p.Pro1050Arg
|
|
|
NM_001289937.2:c.3159+326C>G
|
NP_001276866.1:n.3159+326C>G
|
|
|
NM_001382782.1:c.3104C>G
|
NP_001369711.1:p.Pro1035Arg
|
|
|
NM_001382783.1:c.3104C>G
|
NP_001369712.1:p.Pro1035Arg
|
|
|
NM_001382784.1:c.3311C>G
|
NP_001369713.1:p.Pro1104Arg
|
|
|
NM_001382785.1:c.3296C>G
|
NP_001369714.1:p.Pro1099Arg
|
|
|
NM_001382786.1:c.3275C>G
|
NP_001369715.1:p.Pro1092Arg
|
|
|
NM_001382787.1:c.3269C>G
|
NP_001369716.1:p.Pro1090Arg
|
|
|
NM_001382788.1:c.3224C>G
|
NP_001369717.1:p.Pro1075Arg
|
|
|
NM_001382789.1:c.3215C>G
|
NP_001369718.1:p.Pro1072Arg
|
|
|
NM_001382790.1:c.3191C>G
|
NP_001369719.1:p.Pro1064Arg
|
|
|
NM_001382791.1:c.3185C>G
|
NP_001369720.1:p.Pro1062Arg
|
|
|
NM_001382792.1:c.3158C>G
|
NP_001369721.1:p.Pro1053Arg
|
|
|
NM_001382793.1:c.3152C>G
|
NP_001369722.1:p.Pro1051Arg
|
|
|
NM_001382794.1:c.3152C>G
|
NP_001369723.1:p.Pro1051Arg
|
|
|
NM_001382795.1:c.3146C>G
|
NP_001369724.1:p.Pro1049Arg
|
|
|
NM_001382796.1:c.3107C>G
|
NP_001369725.1:p.Pro1036Arg
|
|
|
NM_001382797.1:c.3095C>G
|
NP_001369726.1:p.Pro1032Arg
|
|
|
NM_001382798.1:c.3038C>G
|
NP_001369727.1:p.Pro1013Arg
|
|
|
NM_001382799.1:c.3014C>G
|
NP_001369728.1:p.Pro1005Arg
|
|
|
NM_001382800.1:c.3008C>G
|
NP_001369729.1:p.Pro1003Arg
|
|
|
NM_001382801.1:c.2990C>G
|
NP_001369730.1:p.Pro997Arg
|
|
|
NM_001382802.1:c.2936C>G
|
NP_001369731.1:p.Pro979Arg
|
|
|
NM_001382803.1:c.3117+326C>G
|
NP_001369732.1:n.3117+326C>G
|
|
|
NM_001382804.1:c.2366C>G
|
NP_001369733.1:p.Pro789Arg
|
|
|
NM_001382805.1:c.2243C>G
|
NP_001369734.1:p.Pro748Arg
|
|
|
NM_001382806.1:c.2156C>G
|
NP_001369735.1:p.Pro719Arg
|
|
|
NM_004448.4:c.3194C>G
MANE Select
|
NP_004439.2:p.Pro1065Arg
|
|
|
NR_110535.2:n.3432C>G
|
|
|
