ENST00000685708.1:n.2827C>T
|
|
|
ENST00000685801.1:c.*511C>T
|
ENSP00000510688.1:n.*511C>T
|
|
ENST00000690244.1:n.1730C>T
|
|
|
ENST00000691109.1:n.6689C>T
|
|
|
ENST00000216181.11:c.*511C>T
MANE Select
|
ENSP00000216181.6:n.*511C>T
|
|
ENST00000216181.9:c.*511C>T
|
ENSP00000216181.5:n.*511C>T
|
|
NM_002473.5:c.*511C>T , LRG_567t1:c.*511C>T
|
NP_002464.1:n.*511C>T
|
|
XM_011530197.1:c.*511C>T
|
XP_011528499.1:n.*511C>T
|
|
XM_011530197.2:c.*511C>T
|
XP_011528499.1:n.*511C>T
|
|
XM_017028803.1:c.*511C>T
|
XP_016884292.1:n.*511C>T
|
|
XM_017028804.1:c.*511C>T
|
XP_016884293.1:n.*511C>T
|
|
XM_017028805.1:c.*511C>T
|
XP_016884294.1:n.*511C>T
|
|
XM_017028806.1:c.*511C>T
|
XP_016884295.1:n.*511C>T
|
|
NM_002473.6:c.*511C>T
MANE Select
|
NP_002464.1:n.*511C>T
|
|