|
NM_004448.4:c.2185G>T
MANE Select
|
NP_004439.2:p.Gly729Cys
|
|
ENST00000269571.10:c.2185G>T
MANE Select
|
ENSP00000269571.4:p.Gly729Cys
|
|
NM_001005862.2:c.2095G>T , LRG_724t1:c.2095G>T
|
NP_001005862.1:p.Gly699Cys
|
|
NM_001005862.3:c.2095G>T
|
NP_001005862.1:p.Gly699Cys
|
|
NM_001289936.1:c.2140G>T , LRG_724t4:c.2140G>T
|
NP_001276865.1:p.Gly714Cys
|
|
NM_001289936.2:c.2140G>T
|
NP_001276865.1:p.Gly714Cys
|
|
NM_001289937.1:c.2185G>T
|
NP_001276866.1:p.Gly729Cys
|
|
NM_001289937.2:c.2185G>T
|
NP_001276866.1:p.Gly729Cys
|
|
NM_001382782.1:c.2095G>T
|
NP_001369711.1:p.Gly699Cys
|
|
NM_001382783.1:c.2095G>T
|
NP_001369712.1:p.Gly699Cys
|
|
NM_001382784.1:c.2302G>T
|
NP_001369713.1:p.Gly768Cys
|
|
NM_001382785.1:c.2287G>T
|
NP_001369714.1:p.Gly763Cys
|
|
NM_001382786.1:c.2289+13G>T
|
NP_001369715.1:n.2289+13G>T
|
|
NM_001382787.1:c.2260G>T
|
NP_001369716.1:p.Gly754Cys
|
|
NM_001382788.1:c.2215G>T
|
NP_001369717.1:p.Gly739Cys
|
|
NM_001382789.1:c.2206G>T
|
NP_001369718.1:p.Gly736Cys
|
|
NM_001382790.1:c.2182G>T
|
NP_001369719.1:p.Gly728Cys
|
|
NM_001382791.1:c.2176G>T
|
NP_001369720.1:p.Gly726Cys
|
|
NM_001382792.1:c.2172+13G>T
|
NP_001369721.1:n.2172+13G>T
|
|
NM_001382793.1:c.2166+19G>T
|
NP_001369722.1:n.2166+19G>T
|
|
NM_001382794.1:c.2143G>T
|
NP_001369723.1:p.Gly715Cys
|
|
NM_001382795.1:c.2137G>T
|
NP_001369724.1:p.Gly713Cys
|
|
NM_001382796.1:c.2185G>T
|
NP_001369725.1:p.Gly729Cys
|
|
NM_001382797.1:c.2185G>T
|
NP_001369726.1:p.Gly729Cys
|
|
NM_001382798.1:c.2185G>T
|
NP_001369727.1:p.Gly729Cys
|
|
NM_001382799.1:c.2005G>T
|
NP_001369728.1:p.Gly669Cys
|
|
NM_001382800.1:c.2185G>T
|
NP_001369729.1:p.Gly729Cys
|
|
NM_001382801.1:c.2137G>T
|
NP_001369730.1:p.Gly713Cys
|
|
NM_001382802.1:c.1927G>T
|
NP_001369731.1:p.Gly643Cys
|
|
NM_001382803.1:c.2166+19G>T
|
NP_001369732.1:n.2166+19G>T
|
|
NM_001382804.1:c.1357G>T
|
NP_001369733.1:p.Gly453Cys
|
|
NM_001382805.1:c.2185G>T
|
NP_001369734.1:p.Gly729Cys
|
|
NM_001382806.1:c.1223-327G>T
|
NP_001369735.1:n.1223-327G>T
|
|
NM_004448.3:c.2185G>T , LRG_724t2:c.2185G>T
|
NP_004439.2:p.Gly729Cys
|
|
NR_110535.1:n.2509G>T
|
|
|
NR_110535.2:n.2423G>T
|
|
|
ENST00000269571.9:c.2185G>T
|
ENSP00000269571.4:p.Gly729Cys
|
|
ENST00000406381.6:c.2095G>T
|
ENSP00000385185.2:p.Gly699Cys
|
|
ENST00000445658.6:c.1357G>T
|
ENSP00000404047.2:p.Gly453Cys
|
|
ENST00000541774.5:c.2140G>T
|
ENSP00000446466.1:p.Gly714Cys
|
|
ENST00000578373.5:c.*1975G>T
|
ENSP00000463427.1:n.*1975G>T
|
|
ENST00000578630.1:n.794G>T
|
|
|
ENST00000580074.1:c.291G>T
|
|
|
ENST00000582818.5:c.490+13G>T
|
|
|
ENST00000583038.5:n.3319G>T
|
|
|
ENST00000584450.5:c.2185G>T
|
ENSP00000463714.1:p.Gly729Cys
|
|
ENST00000584601.5:c.2095G>T
|
ENSP00000462438.1:p.Gly699Cys
|
|
XM_024450641.1:c.2323G>T
|
XP_024306409.1:p.Gly775Cys
|
|
XM_024450642.1:c.2278G>T
|
XP_024306410.1:p.Gly760Cys
|
|
XM_024450643.1:c.2233G>T
|
XP_024306411.1:p.Gly745Cys
|
