ENST00000261275.5:c.277-55321G>C
MANE Select
|
ENSP00000261275.4:n.277-55321G>C
|
|
ENST00000261275.4:c.277-55321G>C
|
ENSP00000261275.4:n.277-55321G>C
|
|
ENST00000560082.1:c.-12-55321G>C
|
ENSP00000452860.1:n.-12-55321G>C
|
|
NM_015307.1:c.277-55321G>C
|
NP_056122.1:n.277-55321G>C
|
|
XM_011521407.1:c.160-55321G>C
|
XP_011519709.1:n.160-55321G>C
|
|
XM_011521407.2:c.160-55321G>C
|
XP_011519709.1:n.160-55321G>C
|
|
NM_001387214.1:c.277-55321G>C
|
NP_001374143.1:n.277-55321G>C
|
|
NM_001387215.1:c.-12-55321G>C
|
NP_001374144.1:n.-12-55321G>C
|
|
NM_001387216.1:c.-12-55321G>C
|
NP_001374145.1:n.-12-55321G>C
|
|
NM_001387217.1:c.-12-55321G>C
|
NP_001374146.1:n.-12-55321G>C
|
|
NM_015307.2:c.277-55321G>C
MANE Select
|
NP_056122.1:n.277-55321G>C
|
|