ENST00000260197.12:c.*1483G>T
MANE Select
|
ENSP00000260197.6:n.*1483G>T
|
|
ENST00000260197.11:c.*1483G>T
|
ENSP00000260197.6:n.*1483G>T
|
|
ENST00000530365.1:n.759-970G>T
|
|
|
NM_003105.5:c.*1483G>T
|
NP_003096.1:n.*1483G>T
|
|
XM_011542963.1:c.*1483G>T
|
XP_011541265.1:n.*1483G>T
|
|
XM_011542965.1:c.*1483G>T
|
XP_011541267.1:n.*1483G>T
|
|
XM_011542966.1:c.*1483G>T
|
XP_011541268.1:n.*1483G>T
|
|
XM_011542967.1:c.*1483G>T
|
XP_011541269.1:n.*1483G>T
|
|
XM_011542965.3:c.*1483G>T
|
XP_011541267.1:n.*1483G>T
|
|
XM_011542967.3:c.*1483G>T
|
XP_011541269.1:n.*1483G>T
|
|
XM_017018172.2:c.*1483G>T
|
XP_016873661.1:n.*1483G>T
|
|
NM_003105.6:c.*1483G>T
MANE Select
|
NP_003096.2:n.*1483G>T
|
|