ENST00000264638.9:c.-189A>G
(CNTNAP1)
MANE Select
|
ENSP00000264638.3:n.-189A>G
|
|
ENST00000264638.8:c.-189A>G
(CNTNAP1)
|
ENSP00000264638.3:n.-189A>G
|
|
ENST00000591568.1:c.-643+1175T>C
(CCR10)
|
ENSP00000467331.1:n.-643+1175T>C
|
|
ENST00000591765.1:c.-963T>C
(CCR10)
|
ENSP00000468135.1:n.-963T>C
|
|
NM_003632.2:c.-189A>G
(CNTNAP1)
|
NP_003623.1:n.-189A>G
|
|
XM_005257748.4:c.-1209A>G
(CNTNAP1)
|
XP_005257805.1:n.-1209A>G
|
|
XM_017025238.1:c.-189A>G
(CNTNAP1)
|
XP_016880727.1:n.-189A>G
|
|
XM_024451011.1:c.-189A>G
(CNTNAP1)
|
XP_024306779.1:n.-189A>G
|
|
NM_003632.3:c.-189A>G
(CNTNAP1)
MANE Select
|
NP_003623.1:n.-189A>G
|
|