ENST00000325321.8:c.*1056G>T
MANE Select
|
ENSP00000313581.2:n.*1056G>T
|
|
ENST00000325321.7:c.*1056G>T
|
ENSP00000313581.2:n.*1056G>T
|
|
ENST00000358049.8:c.*1207G>T
|
ENSP00000350748.3:n.*1207G>T
|
|
ENST00000391810.6:c.*1056G>T
|
ENSP00000375686.2:n.*1056G>T
|
|
ENST00000597439.1:c.*1371G>T
|
ENSP00000471214.1:n.*1371G>T
|
|
NM_001002231.2:c.*1207G>T
|
NP_001002231.1:n.*1207G>T
|
|
NM_001256080.1:c.*1056G>T
|
NP_001243009.1:n.*1056G>T
|
|
NM_005551.4:c.*1056G>T
|
NP_005542.1:n.*1056G>T
|
|
NR_045762.1:n.1907G>T
|
|
|
NR_045763.1:n.1969G>T
|
|
|
NM_005551.5:c.*1056G>T
MANE Select
|
NP_005542.1:n.*1056G>T
|
|
NM_001002231.3:c.*1207G>T
|
NP_001002231.1:n.*1207G>T
|
|
NR_045762.2:n.1901G>T
|
|
|
NR_045763.2:n.1963G>T
|
|
|
NM_001256080.2:c.*1056G>T
|
NP_001243009.1:n.*1056G>T
|
|