ENST00000225964.10:c.1767+322T>C
MANE Select
|
ENSP00000225964.6:n.1767+322T>C
|
|
ENST00000225964.9:c.1767+322T>C
|
ENSP00000225964.5:n.1767+322T>C
|
|
ENST00000463440.1:n.479T>C
|
|
|
ENST00000471344.1:n.1121T>C
|
|
|
ENST00000476387.1:n.116+322T>C
|
|
|
NM_000088.3:c.1767+322T>C , LRG_1t1:c.1767+322T>C
|
NP_000079.2:n.1767+322T>C
|
|
XM_005257058.3:c.1767+322T>C
|
XP_005257115.2:n.1767+322T>C
|
|
XM_005257059.3:c.958-928T>C
|
XP_005257116.2:n.958-928T>C
|
|
XM_011524341.1:c.1569+322T>C
|
XP_011522643.1:n.1569+322T>C
|
|
XM_005257058.4:c.1767+322T>C
|
XP_005257115.2:n.1767+322T>C
|
|
XM_005257059.4:c.958-928T>C
|
XP_005257116.2:n.958-928T>C
|
|
NM_000088.4:c.1767+322T>C
MANE Select
|
NP_000079.2:n.1767+322T>C
|
|