ENST00000646743.1:c.*391C>T
MANE Select
|
ENSP00000495564.1:n.*391C>T
|
|
ENST00000251808.7:c.*391C>T
|
ENSP00000251808.3:n.*391C>T
|
|
NM_024915.3:c.*391C>T
|
NP_079191.2:n.*391C>T
|
|
XM_011517305.1:c.*391C>T
|
XP_011515607.1:n.*391C>T
|
|
XM_011517306.1:c.*391C>T
|
XP_011515608.1:n.*391C>T
|
|
XM_011517307.1:c.1763+2576C>T
|
XP_011515609.1:n.1763+2576C>T
|
|
NM_001330593.1:c.*391C>T
|
NP_001317522.1:n.*391C>T
|
|
XM_011517306.3:c.*391C>T
|
XP_011515608.1:n.*391C>T
|
|
XM_011517307.3:c.1763+2576C>T
|
XP_011515609.1:n.1763+2576C>T
|
|
NM_001330593.2:c.*391C>T
|
NP_001317522.1:n.*391C>T
|
|
NM_024915.4:c.*391C>T
MANE Select
|
NP_079191.2:n.*391C>T
|
|