ENST00000264638.9:c.-207G>T
(CNTNAP1)
MANE Select
|
ENSP00000264638.3:n.-207G>T
|
|
ENST00000264638.8:c.-207G>T
(CNTNAP1)
|
ENSP00000264638.3:n.-207G>T
|
|
ENST00000591568.1:c.-643+1193C>A
(CCR10)
|
ENSP00000467331.1:n.-643+1193C>A
|
|
ENST00000591765.1:c.-945C>A
(CCR10)
|
ENSP00000468135.1:n.-945C>A
|
|
NM_003632.2:c.-207G>T
(CNTNAP1)
|
NP_003623.1:n.-207G>T
|
|
XM_017025238.1:c.-207G>T
(CNTNAP1)
|
XP_016880727.1:n.-207G>T
|
|
XM_024451011.1:c.-207G>T
(CNTNAP1)
|
XP_024306779.1:n.-207G>T
|
|
NM_003632.3:c.-207G>T
(CNTNAP1)
MANE Select
|
NP_003623.1:n.-207G>T
|
|