ENST00000646743.1:c.1612+2T>G
MANE Select
|
ENSP00000495564.1:n.1612+2T>G
|
|
ENST00000251808.7:c.1612+2T>G
|
ENSP00000251808.3:n.1612+2T>G
|
|
ENST00000395927.1:c.1564+2T>G
|
ENSP00000379260.1:n.1564+2T>G
|
|
ENST00000474338.1:n.254+2T>G
|
|
|
ENST00000517674.5:n.267+2T>G
|
|
|
NM_024915.3:c.1612+2T>G
|
NP_079191.2:n.1612+2T>G
|
|
XM_011517305.1:c.1564+2T>G
|
XP_011515607.1:n.1564+2T>G
|
|
XM_011517306.1:c.1564+2T>G
|
XP_011515608.1:n.1564+2T>G
|
|
XM_011517307.1:c.1612+2T>G
|
XP_011515609.1:n.1612+2T>G
|
|
NM_001330593.1:c.1564+2T>G
|
NP_001317522.1:n.1564+2T>G
|
|
XM_011517306.3:c.1564+2T>G
|
XP_011515608.1:n.1564+2T>G
|
|
XM_011517307.3:c.1612+2T>G
|
XP_011515609.1:n.1612+2T>G
|
|
NM_001330593.2:c.1564+2T>G
|
NP_001317522.1:n.1564+2T>G
|
|
NM_024915.4:c.1612+2T>G
MANE Select
|
NP_079191.2:n.1612+2T>G
|
|