ENST00000061240.7:c.1847-38A=
MANE Select
|
ENSP00000061240.2:n.1847-38A=
|
|
ENST00000061240.6:c.1847-38A=
|
ENSP00000061240.2:n.1847-38A=
|
|
ENST00000507499.5:c.1916-38A=
|
ENSP00000426082.1:n.1916-38A=
|
|
ENST00000509505.5:c.*1492-38A=
|
ENSP00000422692.1:n.*1492-38A=
|
|
NM_012464.4:c.1847-38A=
|
NP_036596.3:n.1847-38A=
|
|
XM_011532212.1:c.1847-38A=
|
XP_011530514.1:n.1847-38A=
|
|
XM_011532213.1:c.1700-38A=
|
XP_011530515.1:n.1700-38A=
|
|
XM_011532214.1:c.1319-38A=
|
XP_011530516.1:n.1319-38A=
|
|
XM_017008570.1:c.1700-38A=
|
XP_016864059.1:n.1700-38A=
|
|
XM_024454194.1:c.1547-38A=
|
XP_024309962.1:n.1547-38A=
|
|
XM_024454195.1:c.1547-38A=
|
XP_024309963.1:n.1547-38A=
|
|
NM_012464.5:c.1847-38A=
MANE Select
|
NP_036596.3:n.1847-38A=
|
|