ENST00000269571.10:c.3643C>T
MANE Select
|
ENSP00000269571.4:p.Pro1215Ser
|
|
ENST00000269571.9:c.3643C>T
|
ENSP00000269571.4:p.Pro1215Ser
|
|
ENST00000406381.6:c.3553C>T
|
ENSP00000385185.2:p.Pro1185Ser
|
|
ENST00000445658.6:c.2815C>T
|
ENSP00000404047.2:p.Pro939Ser
|
|
ENST00000541774.5:c.3598C>T
|
ENSP00000446466.1:p.Pro1200Ser
|
|
ENST00000578373.5:c.*3433C>T
|
ENSP00000463427.1:n.*3433C>T
|
|
ENST00000584450.5:c.*222C>T
|
ENSP00000463714.1:n.*222C>T
|
|
ENST00000584601.5:c.3553C>T
|
ENSP00000462438.1:p.Pro1185Ser
|
|
NM_001005862.2:c.3553C>T , LRG_724t1:c.3553C>T
|
NP_001005862.1:p.Pro1185Ser
|
|
NM_001289936.1:c.3598C>T , LRG_724t4:c.3598C>T
|
NP_001276865.1:p.Pro1200Ser
|
|
NM_001289937.1:c.*222C>T
|
NP_001276866.1:n.*222C>T
|
|
NM_004448.3:c.3643C>T , LRG_724t2:c.3643C>T
|
NP_004439.2:p.Pro1215Ser
|
|
NR_110535.1:n.3967C>T
|
|
|
XM_024450641.1:c.3781C>T
|
XP_024306409.1:p.Pro1261Ser
|
|
XM_024450642.1:c.3736C>T
|
XP_024306410.1:p.Pro1246Ser
|
|
XM_024450643.1:c.3691C>T
|
XP_024306411.1:p.Pro1231Ser
|
|
NM_001005862.3:c.3553C>T
|
NP_001005862.1:p.Pro1185Ser
|
|
NM_001289936.2:c.3598C>T
|
NP_001276865.1:p.Pro1200Ser
|
|
NM_001289937.2:c.*222C>T
|
NP_001276866.1:n.*222C>T
|
|
NM_001382782.1:c.3553C>T
|
NP_001369711.1:p.Pro1185Ser
|
|
NM_001382783.1:c.3553C>T
|
NP_001369712.1:p.Pro1185Ser
|
|
NM_001382784.1:c.3760C>T
|
NP_001369713.1:p.Pro1254Ser
|
|
NM_001382785.1:c.3745C>T
|
NP_001369714.1:p.Pro1249Ser
|
|
NM_001382786.1:c.3724C>T
|
NP_001369715.1:p.Pro1242Ser
|
|
NM_001382787.1:c.3718C>T
|
NP_001369716.1:p.Pro1240Ser
|
|
NM_001382788.1:c.3673C>T
|
NP_001369717.1:p.Pro1225Ser
|
|
NM_001382789.1:c.3664C>T
|
NP_001369718.1:p.Pro1222Ser
|
|
NM_001382790.1:c.3640C>T
|
NP_001369719.1:p.Pro1214Ser
|
|
NM_001382791.1:c.3634C>T
|
NP_001369720.1:p.Pro1212Ser
|
|
NM_001382792.1:c.3607C>T
|
NP_001369721.1:p.Pro1203Ser
|
|
NM_001382793.1:c.3601C>T
|
NP_001369722.1:p.Pro1201Ser
|
|
NM_001382794.1:c.3601C>T
|
NP_001369723.1:p.Pro1201Ser
|
|
NM_001382795.1:c.3595C>T
|
NP_001369724.1:p.Pro1199Ser
|
|
NM_001382796.1:c.3556C>T
|
NP_001369725.1:p.Pro1186Ser
|
|
NM_001382797.1:c.3544C>T
|
NP_001369726.1:p.Pro1182Ser
|
|
NM_001382798.1:c.3487C>T
|
NP_001369727.1:p.Pro1163Ser
|
|
NM_001382799.1:c.3463C>T
|
NP_001369728.1:p.Pro1155Ser
|
|
NM_001382800.1:c.3457C>T
|
NP_001369729.1:p.Pro1153Ser
|
|
NM_001382801.1:c.3439C>T
|
NP_001369730.1:p.Pro1147Ser
|
|
NM_001382802.1:c.3385C>T
|
NP_001369731.1:p.Pro1129Ser
|
|
NM_001382803.1:c.*222C>T
|
NP_001369732.1:n.*222C>T
|
|
NM_001382804.1:c.2815C>T
|
NP_001369733.1:p.Pro939Ser
|
|
NM_001382805.1:c.2692C>T
|
NP_001369734.1:p.Pro898Ser
|
|
NM_001382806.1:c.2605C>T
|
NP_001369735.1:p.Pro869Ser
|
|
NM_004448.4:c.3643C>T
MANE Select
|
NP_004439.2:p.Pro1215Ser
|
|
NR_110535.2:n.3881C>T
|
|
|