ENST00000269571.10:c.3523C>T
MANE Select
|
ENSP00000269571.4:p.Pro1175Ser
|
|
ENST00000269571.9:c.3523C>T
|
ENSP00000269571.4:p.Pro1175Ser
|
|
ENST00000406381.6:c.3433C>T
|
ENSP00000385185.2:p.Pro1145Ser
|
|
ENST00000445658.6:c.2695C>T
|
ENSP00000404047.2:p.Pro899Ser
|
|
ENST00000541774.5:c.3478C>T
|
ENSP00000446466.1:p.Pro1160Ser
|
|
ENST00000578373.5:c.*3313C>T
|
ENSP00000463427.1:n.*3313C>T
|
|
ENST00000584450.5:c.*102C>T
|
ENSP00000463714.1:n.*102C>T
|
|
ENST00000584601.5:c.3433C>T
|
ENSP00000462438.1:p.Pro1145Ser
|
|
NM_001005862.2:c.3433C>T , LRG_724t1:c.3433C>T
|
NP_001005862.1:p.Pro1145Ser
|
|
NM_001289936.1:c.3478C>T , LRG_724t4:c.3478C>T
|
NP_001276865.1:p.Pro1160Ser
|
|
NM_001289937.1:c.*102C>T
|
NP_001276866.1:n.*102C>T
|
|
NM_004448.3:c.3523C>T , LRG_724t2:c.3523C>T
|
NP_004439.2:p.Pro1175Ser
|
|
NR_110535.1:n.3847C>T
|
|
|
XM_024450641.1:c.3661C>T
|
XP_024306409.1:p.Pro1221Ser
|
|
XM_024450642.1:c.3616C>T
|
XP_024306410.1:p.Pro1206Ser
|
|
XM_024450643.1:c.3571C>T
|
XP_024306411.1:p.Pro1191Ser
|
|
NM_001005862.3:c.3433C>T
|
NP_001005862.1:p.Pro1145Ser
|
|
NM_001289936.2:c.3478C>T
|
NP_001276865.1:p.Pro1160Ser
|
|
NM_001289937.2:c.*102C>T
|
NP_001276866.1:n.*102C>T
|
|
NM_001382782.1:c.3433C>T
|
NP_001369711.1:p.Pro1145Ser
|
|
NM_001382783.1:c.3433C>T
|
NP_001369712.1:p.Pro1145Ser
|
|
NM_001382784.1:c.3640C>T
|
NP_001369713.1:p.Pro1214Ser
|
|
NM_001382785.1:c.3625C>T
|
NP_001369714.1:p.Pro1209Ser
|
|
NM_001382786.1:c.3604C>T
|
NP_001369715.1:p.Pro1202Ser
|
|
NM_001382787.1:c.3598C>T
|
NP_001369716.1:p.Pro1200Ser
|
|
NM_001382788.1:c.3553C>T
|
NP_001369717.1:p.Pro1185Ser
|
|
NM_001382789.1:c.3544C>T
|
NP_001369718.1:p.Pro1182Ser
|
|
NM_001382790.1:c.3520C>T
|
NP_001369719.1:p.Pro1174Ser
|
|
NM_001382791.1:c.3514C>T
|
NP_001369720.1:p.Pro1172Ser
|
|
NM_001382792.1:c.3487C>T
|
NP_001369721.1:p.Pro1163Ser
|
|
NM_001382793.1:c.3481C>T
|
NP_001369722.1:p.Pro1161Ser
|
|
NM_001382794.1:c.3481C>T
|
NP_001369723.1:p.Pro1161Ser
|
|
NM_001382795.1:c.3475C>T
|
NP_001369724.1:p.Pro1159Ser
|
|
NM_001382796.1:c.3436C>T
|
NP_001369725.1:p.Pro1146Ser
|
|
NM_001382797.1:c.3424C>T
|
NP_001369726.1:p.Pro1142Ser
|
|
NM_001382798.1:c.3367C>T
|
NP_001369727.1:p.Pro1123Ser
|
|
NM_001382799.1:c.3343C>T
|
NP_001369728.1:p.Pro1115Ser
|
|
NM_001382800.1:c.3337C>T
|
NP_001369729.1:p.Pro1113Ser
|
|
NM_001382801.1:c.3319C>T
|
NP_001369730.1:p.Pro1107Ser
|
|
NM_001382802.1:c.3265C>T
|
NP_001369731.1:p.Pro1089Ser
|
|
NM_001382803.1:c.*102C>T
|
NP_001369732.1:n.*102C>T
|
|
NM_001382804.1:c.2695C>T
|
NP_001369733.1:p.Pro899Ser
|
|
NM_001382805.1:c.2572C>T
|
NP_001369734.1:p.Pro858Ser
|
|
NM_001382806.1:c.2485C>T
|
NP_001369735.1:p.Pro829Ser
|
|
NM_004448.4:c.3523C>T
MANE Select
|
NP_004439.2:p.Pro1175Ser
|
|
NR_110535.2:n.3761C>T
|
|
|