ENST00000419482.7:c.138-2099T>G
MANE Select
|
ENSP00000393453.2:n.138-2099T>G
|
|
ENST00000419482.6:c.138-2099T>G
|
ENSP00000393453.2:n.138-2099T>G
|
|
ENST00000438570.1:c.138-2099T>G
|
ENSP00000387482.1:n.138-2099T>G
|
|
ENST00000444564.2:c.138-2099T>G
|
ENSP00000407888.2:n.138-2099T>G
|
|
NM_198274.3:c.138-2099T>G
|
NP_938015.1:n.138-2099T>G
|
|
XM_005264156.2:c.138-2099T>G
|
XP_005264213.1:n.138-2099T>G
|
|
NM_001330364.1:c.138-2099T>G
|
NP_001317293.1:n.138-2099T>G
|
|
NM_198274.4:c.138-2099T>G
MANE Select
|
NP_938015.1:n.138-2099T>G
|
|
NM_001330364.2:c.138-2099T>G
|
NP_001317293.1:n.138-2099T>G
|
|