|
ENST00000269571.10:c.3195C>G
MANE Select
|
ENSP00000269571.4:p.Pro1065=
|
|
|
ENST00000269571.9:c.3195C>G
|
ENSP00000269571.4:p.Pro1065=
|
|
|
ENST00000406381.6:c.3105C>G
|
ENSP00000385185.2:p.Pro1035=
|
|
|
ENST00000445658.6:c.2367C>G
|
ENSP00000404047.2:p.Pro789=
|
|
|
ENST00000541774.5:c.3150C>G
|
ENSP00000446466.1:p.Pro1050=
|
|
|
ENST00000578373.5:c.*2985C>G
|
ENSP00000463427.1:n.*2985C>G
|
|
|
ENST00000584450.5:c.3159+327C>G
|
ENSP00000463714.1:n.3159+327C>G
|
|
|
ENST00000584601.5:c.3105C>G
|
ENSP00000462438.1:p.Pro1035=
|
|
|
NM_001005862.2:c.3105C>G , LRG_724t1:c.3105C>G
|
NP_001005862.1:p.Pro1035=
|
|
|
NM_001289936.1:c.3150C>G , LRG_724t4:c.3150C>G
|
NP_001276865.1:p.Pro1050=
|
|
|
NM_001289937.1:c.3159+327C>G
|
NP_001276866.1:n.3159+327C>G
|
|
|
NM_004448.3:c.3195C>G , LRG_724t2:c.3195C>G
|
NP_004439.2:p.Pro1065=
|
|
|
NR_110535.1:n.3519C>G
|
|
|
|
XM_024450641.1:c.3333C>G
|
XP_024306409.1:p.Pro1111=
|
|
|
XM_024450642.1:c.3288C>G
|
XP_024306410.1:p.Pro1096=
|
|
|
XM_024450643.1:c.3243C>G
|
XP_024306411.1:p.Pro1081=
|
|
|
NM_001005862.3:c.3105C>G
|
NP_001005862.1:p.Pro1035=
|
|
|
NM_001289936.2:c.3150C>G
|
NP_001276865.1:p.Pro1050=
|
|
|
NM_001289937.2:c.3159+327C>G
|
NP_001276866.1:n.3159+327C>G
|
|
|
NM_001382782.1:c.3105C>G
|
NP_001369711.1:p.Pro1035=
|
|
|
NM_001382783.1:c.3105C>G
|
NP_001369712.1:p.Pro1035=
|
|
|
NM_001382784.1:c.3312C>G
|
NP_001369713.1:p.Pro1104=
|
|
|
NM_001382785.1:c.3297C>G
|
NP_001369714.1:p.Pro1099=
|
|
|
NM_001382786.1:c.3276C>G
|
NP_001369715.1:p.Pro1092=
|
|
|
NM_001382787.1:c.3270C>G
|
NP_001369716.1:p.Pro1090=
|
|
|
NM_001382788.1:c.3225C>G
|
NP_001369717.1:p.Pro1075=
|
|
|
NM_001382789.1:c.3216C>G
|
NP_001369718.1:p.Pro1072=
|
|
|
NM_001382790.1:c.3192C>G
|
NP_001369719.1:p.Pro1064=
|
|
|
NM_001382791.1:c.3186C>G
|
NP_001369720.1:p.Pro1062=
|
|
|
NM_001382792.1:c.3159C>G
|
NP_001369721.1:p.Pro1053=
|
|
|
NM_001382793.1:c.3153C>G
|
NP_001369722.1:p.Pro1051=
|
|
|
NM_001382794.1:c.3153C>G
|
NP_001369723.1:p.Pro1051=
|
|
|
NM_001382795.1:c.3147C>G
|
NP_001369724.1:p.Pro1049=
|
|
|
NM_001382796.1:c.3108C>G
|
NP_001369725.1:p.Pro1036=
|
|
|
NM_001382797.1:c.3096C>G
|
NP_001369726.1:p.Pro1032=
|
|
|
NM_001382798.1:c.3039C>G
|
NP_001369727.1:p.Pro1013=
|
|
|
NM_001382799.1:c.3015C>G
|
NP_001369728.1:p.Pro1005=
|
|
|
NM_001382800.1:c.3009C>G
|
NP_001369729.1:p.Pro1003=
|
|
|
NM_001382801.1:c.2991C>G
|
NP_001369730.1:p.Pro997=
|
|
|
NM_001382802.1:c.2937C>G
|
NP_001369731.1:p.Pro979=
|
|
|
NM_001382803.1:c.3117+327C>G
|
NP_001369732.1:n.3117+327C>G
|
|
|
NM_001382804.1:c.2367C>G
|
NP_001369733.1:p.Pro789=
|
|
|
NM_001382805.1:c.2244C>G
|
NP_001369734.1:p.Pro748=
|
|
|
NM_001382806.1:c.2157C>G
|
NP_001369735.1:p.Pro719=
|
|
|
NM_004448.4:c.3195C>G
MANE Select
|
NP_004439.2:p.Pro1065=
|
|
|
NR_110535.2:n.3433C>G
|
|
|
