ENST00000409155.8:c.931+21T>G
MANE Select
|
ENSP00000386284.3:n.931+21T>G
|
|
ENST00000409155.7:c.931+21T>G
|
ENSP00000386284.3:n.931+21T>G
|
|
ENST00000482847.5:n.1204+21T>G
|
|
|
NM_000031.5:c.931+21T>G
|
NP_000022.3:n.931+21T>G
|
|
XM_005251799.1:c.1018+21T>G
|
XP_005251856.1:n.1018+21T>G
|
|
XM_011518363.1:c.1057+21T>G
|
XP_011516665.1:n.1057+21T>G
|
|
XM_011518364.1:c.958+21T>G
|
XP_011516666.1:n.958+21T>G
|
|
NM_001003945.2:c.1018+21T>G
|
NP_001003945.1:n.1018+21T>G
|
|
NM_001317745.1:c.907+21T>G
|
NP_001304674.1:n.907+21T>G
|
|
XM_011518364.2:c.958+21T>G
|
XP_011516666.1:n.958+21T>G
|
|
XM_024447449.1:c.1018+21T>G
|
XP_024303217.1:n.1018+21T>G
|
|
NM_000031.6:c.931+21T>G
MANE Select
|
NP_000022.3:n.931+21T>G
|
|
NM_001003945.3:c.1018+21T>G
|
NP_001003945.1:n.1018+21T>G
|
|
NM_001317745.2:c.907+21T>G
|
NP_001304674.1:n.907+21T>G
|
|