ENST00000685708.1:n.2748G>T
|
|
|
ENST00000685801.1:c.*432G>T
|
ENSP00000510688.1:n.*432G>T
|
|
ENST00000690244.1:n.1651G>T
|
|
|
ENST00000691109.1:n.6610G>T
|
|
|
ENST00000216181.11:c.*432G>T
MANE Select
|
ENSP00000216181.6:n.*432G>T
|
|
ENST00000216181.9:c.*432G>T
|
ENSP00000216181.5:n.*432G>T
|
|
NM_002473.5:c.*432G>T , LRG_567t1:c.*432G>T
|
NP_002464.1:n.*432G>T
|
|
XM_011530197.1:c.*432G>T
|
XP_011528499.1:n.*432G>T
|
|
XM_011530197.2:c.*432G>T
|
XP_011528499.1:n.*432G>T
|
|
XM_017028803.1:c.*432G>T
|
XP_016884292.1:n.*432G>T
|
|
XM_017028804.1:c.*432G>T
|
XP_016884293.1:n.*432G>T
|
|
XM_017028805.1:c.*432G>T
|
XP_016884294.1:n.*432G>T
|
|
XM_017028806.1:c.*432G>T
|
XP_016884295.1:n.*432G>T
|
|
NM_002473.6:c.*432G>T
MANE Select
|
NP_002464.1:n.*432G>T
|
|