ENST00000334444.11:c.*1243A>T
MANE Select
|
ENSP00000333926.6:n.*1243A>T
|
|
ENST00000265586.10:c.*1243A>T
|
ENSP00000265586.6:n.*1243A>T
|
|
ENST00000334444.10:c.*1243A>T
|
ENSP00000333926.6:n.*1243A>T
|
|
ENST00000437205.5:c.*4250A>T
|
ENSP00000403510.1:n.*4250A>T
|
|
NM_005688.2:c.*1243A>T
|
NP_005679.2:n.*1243A>T
|
|
XM_005247058.3:c.*1243A>T
|
XP_005247115.1:n.*1243A>T
|
|
XM_005247059.3:c.*1243A>T
|
XP_005247116.1:n.*1243A>T
|
|
XM_011512314.1:c.*1243A>T
|
XP_011510616.1:n.*1243A>T
|
|
XM_011512316.1:c.*1243A>T
|
XP_011510618.1:n.*1243A>T
|
|
NM_001320032.1:c.*1243A>T
|
NP_001306961.1:n.*1243A>T
|
|
NM_005688.3:c.*1243A>T
|
NP_005679.2:n.*1243A>T
|
|
XM_005247058.5:c.*1243A>T
|
XP_005247115.1:n.*1243A>T
|
|
XM_005247059.5:c.*1243A>T
|
XP_005247116.1:n.*1243A>T
|
|
XM_011512314.2:c.*1243A>T
|
XP_011510616.1:n.*1243A>T
|
|
XM_017005492.2:c.*1243A>T
|
XP_016860981.1:n.*1243A>T
|
|
XM_024453286.1:c.*1243A>T
|
XP_024309054.1:n.*1243A>T
|
|
NM_005688.4:c.*1243A>T
MANE Select
|
NP_005679.2:n.*1243A>T
|
|
NM_001320032.2:c.*1243A>T
|
NP_001306961.1:n.*1243A>T
|
|