ENST00000269571.10:c.3615T>C
MANE Select
|
ENSP00000269571.4:p.Pro1205=
|
|
ENST00000269571.9:c.3615T>C
|
ENSP00000269571.4:p.Pro1205=
|
|
ENST00000406381.6:c.3525T>C
|
ENSP00000385185.2:p.Pro1175=
|
|
ENST00000445658.6:c.2787T>C
|
ENSP00000404047.2:p.Pro929=
|
|
ENST00000541774.5:c.3570T>C
|
ENSP00000446466.1:p.Pro1190=
|
|
ENST00000578373.5:c.*3405T>C
|
ENSP00000463427.1:n.*3405T>C
|
|
ENST00000584450.5:c.*194T>C
|
ENSP00000463714.1:n.*194T>C
|
|
ENST00000584601.5:c.3525T>C
|
ENSP00000462438.1:p.Pro1175=
|
|
NM_001005862.2:c.3525T>C , LRG_724t1:c.3525T>C
|
NP_001005862.1:p.Pro1175=
|
|
NM_001289936.1:c.3570T>C , LRG_724t4:c.3570T>C
|
NP_001276865.1:p.Pro1190=
|
|
NM_001289937.1:c.*194T>C
|
NP_001276866.1:n.*194T>C
|
|
NM_004448.3:c.3615T>C , LRG_724t2:c.3615T>C
|
NP_004439.2:p.Pro1205=
|
|
NR_110535.1:n.3939T>C
|
|
|
XM_024450641.1:c.3753T>C
|
XP_024306409.1:p.Pro1251=
|
|
XM_024450642.1:c.3708T>C
|
XP_024306410.1:p.Pro1236=
|
|
XM_024450643.1:c.3663T>C
|
XP_024306411.1:p.Pro1221=
|
|
NM_001005862.3:c.3525T>C
|
NP_001005862.1:p.Pro1175=
|
|
NM_001289936.2:c.3570T>C
|
NP_001276865.1:p.Pro1190=
|
|
NM_001289937.2:c.*194T>C
|
NP_001276866.1:n.*194T>C
|
|
NM_001382782.1:c.3525T>C
|
NP_001369711.1:p.Pro1175=
|
|
NM_001382783.1:c.3525T>C
|
NP_001369712.1:p.Pro1175=
|
|
NM_001382784.1:c.3732T>C
|
NP_001369713.1:p.Pro1244=
|
|
NM_001382785.1:c.3717T>C
|
NP_001369714.1:p.Pro1239=
|
|
NM_001382786.1:c.3696T>C
|
NP_001369715.1:p.Pro1232=
|
|
NM_001382787.1:c.3690T>C
|
NP_001369716.1:p.Pro1230=
|
|
NM_001382788.1:c.3645T>C
|
NP_001369717.1:p.Pro1215=
|
|
NM_001382789.1:c.3636T>C
|
NP_001369718.1:p.Pro1212=
|
|
NM_001382790.1:c.3612T>C
|
NP_001369719.1:p.Pro1204=
|
|
NM_001382791.1:c.3606T>C
|
NP_001369720.1:p.Pro1202=
|
|
NM_001382792.1:c.3579T>C
|
NP_001369721.1:p.Pro1193=
|
|
NM_001382793.1:c.3573T>C
|
NP_001369722.1:p.Pro1191=
|
|
NM_001382794.1:c.3573T>C
|
NP_001369723.1:p.Pro1191=
|
|
NM_001382795.1:c.3567T>C
|
NP_001369724.1:p.Pro1189=
|
|
NM_001382796.1:c.3528T>C
|
NP_001369725.1:p.Pro1176=
|
|
NM_001382797.1:c.3516T>C
|
NP_001369726.1:p.Pro1172=
|
|
NM_001382798.1:c.3459T>C
|
NP_001369727.1:p.Pro1153=
|
|
NM_001382799.1:c.3435T>C
|
NP_001369728.1:p.Pro1145=
|
|
NM_001382800.1:c.3429T>C
|
NP_001369729.1:p.Pro1143=
|
|
NM_001382801.1:c.3411T>C
|
NP_001369730.1:p.Pro1137=
|
|
NM_001382802.1:c.3357T>C
|
NP_001369731.1:p.Pro1119=
|
|
NM_001382803.1:c.*194T>C
|
NP_001369732.1:n.*194T>C
|
|
NM_001382804.1:c.2787T>C
|
NP_001369733.1:p.Pro929=
|
|
NM_001382805.1:c.2664T>C
|
NP_001369734.1:p.Pro888=
|
|
NM_001382806.1:c.2577T>C
|
NP_001369735.1:p.Pro859=
|
|
NM_004448.4:c.3615T>C
MANE Select
|
NP_004439.2:p.Pro1205=
|
|
NR_110535.2:n.3853T>C
|
|
|