ENST00000269571.10:c.3684A>T
MANE Select
|
ENSP00000269571.4:p.Pro1228=
|
|
ENST00000269571.9:c.3684A>T
|
ENSP00000269571.4:p.Pro1228=
|
|
ENST00000406381.6:c.3594A>T
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ENSP00000385185.2:p.Pro1198=
|
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ENST00000445658.6:c.2856A>T
|
ENSP00000404047.2:p.Pro952=
|
|
ENST00000541774.5:c.3639A>T
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ENSP00000446466.1:p.Pro1213=
|
|
ENST00000578373.5:c.*3474A>T
|
ENSP00000463427.1:n.*3474A>T
|
|
ENST00000584450.5:c.*263A>T
|
ENSP00000463714.1:n.*263A>T
|
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ENST00000584601.5:c.3594A>T
|
ENSP00000462438.1:p.Pro1198=
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NM_001005862.2:c.3594A>T , LRG_724t1:c.3594A>T
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NP_001005862.1:p.Pro1198=
|
|
NM_001289936.1:c.3639A>T , LRG_724t4:c.3639A>T
|
NP_001276865.1:p.Pro1213=
|
|
NM_001289937.1:c.*263A>T
|
NP_001276866.1:n.*263A>T
|
|
NM_004448.3:c.3684A>T , LRG_724t2:c.3684A>T
|
NP_004439.2:p.Pro1228=
|
|
NR_110535.1:n.4008A>T
|
|
|
XM_024450641.1:c.3822A>T
|
XP_024306409.1:p.Pro1274=
|
|
XM_024450642.1:c.3777A>T
|
XP_024306410.1:p.Pro1259=
|
|
XM_024450643.1:c.3732A>T
|
XP_024306411.1:p.Pro1244=
|
|
NM_001005862.3:c.3594A>T
|
NP_001005862.1:p.Pro1198=
|
|
NM_001289936.2:c.3639A>T
|
NP_001276865.1:p.Pro1213=
|
|
NM_001289937.2:c.*263A>T
|
NP_001276866.1:n.*263A>T
|
|
NM_001382782.1:c.3594A>T
|
NP_001369711.1:p.Pro1198=
|
|
NM_001382783.1:c.3594A>T
|
NP_001369712.1:p.Pro1198=
|
|
NM_001382784.1:c.3801A>T
|
NP_001369713.1:p.Pro1267=
|
|
NM_001382785.1:c.3786A>T
|
NP_001369714.1:p.Pro1262=
|
|
NM_001382786.1:c.3765A>T
|
NP_001369715.1:p.Pro1255=
|
|
NM_001382787.1:c.3759A>T
|
NP_001369716.1:p.Pro1253=
|
|
NM_001382788.1:c.3714A>T
|
NP_001369717.1:p.Pro1238=
|
|
NM_001382789.1:c.3705A>T
|
NP_001369718.1:p.Pro1235=
|
|
NM_001382790.1:c.3681A>T
|
NP_001369719.1:p.Pro1227=
|
|
NM_001382791.1:c.3675A>T
|
NP_001369720.1:p.Pro1225=
|
|
NM_001382792.1:c.3648A>T
|
NP_001369721.1:p.Pro1216=
|
|
NM_001382793.1:c.3642A>T
|
NP_001369722.1:p.Pro1214=
|
|
NM_001382794.1:c.3642A>T
|
NP_001369723.1:p.Pro1214=
|
|
NM_001382795.1:c.3636A>T
|
NP_001369724.1:p.Pro1212=
|
|
NM_001382796.1:c.3597A>T
|
NP_001369725.1:p.Pro1199=
|
|
NM_001382797.1:c.3585A>T
|
NP_001369726.1:p.Pro1195=
|
|
NM_001382798.1:c.3528A>T
|
NP_001369727.1:p.Pro1176=
|
|
NM_001382799.1:c.3504A>T
|
NP_001369728.1:p.Pro1168=
|
|
NM_001382800.1:c.3498A>T
|
NP_001369729.1:p.Pro1166=
|
|
NM_001382801.1:c.3480A>T
|
NP_001369730.1:p.Pro1160=
|
|
NM_001382802.1:c.3426A>T
|
NP_001369731.1:p.Pro1142=
|
|
NM_001382803.1:c.*263A>T
|
NP_001369732.1:n.*263A>T
|
|
NM_001382804.1:c.2856A>T
|
NP_001369733.1:p.Pro952=
|
|
NM_001382805.1:c.2733A>T
|
NP_001369734.1:p.Pro911=
|
|
NM_001382806.1:c.2646A>T
|
NP_001369735.1:p.Pro882=
|
|
NM_004448.4:c.3684A>T
MANE Select
|
NP_004439.2:p.Pro1228=
|
|
NR_110535.2:n.3922A>T
|
|
|