ENST00000620267.2:c.4927-1110G>T
MANE Select
|
ENSP00000480090.1:n.4927-1110G>T
|
|
ENST00000620267.1:c.4927-1110G>T
|
ENSP00000480090.1:n.4927-1110G>T
|
|
NM_181536.1:c.4927-1110G>T
|
NP_853514.1:n.4927-1110G>T
|
|
XM_024450254.1:c.4924-1110G>T
|
XP_024306022.1:n.4924-1110G>T
|
|
XM_024450255.1:c.4909-1110G>T
|
XP_024306023.1:n.4909-1110G>T
|
|
XM_024450256.1:c.4750-1110G>T
|
XP_024306024.1:n.4750-1110G>T
|
|
XM_024450257.1:c.4741-1110G>T
|
XP_024306025.1:n.4741-1110G>T
|
|
XM_024450258.1:c.4375-1110G>T
|
XP_024306026.1:n.4375-1110G>T
|
|
XM_024450259.1:c.4375-1110G>T
|
XP_024306027.1:n.4375-1110G>T
|
|
XM_024450260.1:c.4219-1110G>T
|
XP_024306028.1:n.4219-1110G>T
|
|
NM_181536.2:c.4927-1110G>T
MANE Select
|
NP_853514.1:n.4927-1110G>T
|
|