ENST00000622030.2:c.282-196G>A
MANE Select
|
ENSP00000477587.1:n.282-196G>A
|
|
ENST00000622030.1:c.282-196G>A
|
ENSP00000477587.1:n.282-196G>A
|
|
NM_000348.3:c.282-196G>A
|
NP_000339.2:n.282-196G>A
|
|
XM_011533068.1:c.282-196G>A
|
XP_011531370.1:n.282-196G>A
|
|
XM_011533069.1:c.60-196G>A
|
XP_011531371.1:n.60-196G>A
|
|
XM_011533070.1:c.27-196G>A
|
XP_011531372.1:n.27-196G>A
|
|
XM_011533071.1:c.27-196G>A
|
XP_011531373.1:n.27-196G>A
|
|
XM_011533072.1:c.27-196G>A
|
XP_011531374.1:n.27-196G>A
|
|
XM_011533069.2:c.60-196G>A
|
XP_011531371.1:n.60-196G>A
|
|
XM_011533072.2:c.27-196G>A
|
XP_011531374.1:n.27-196G>A
|
|
NM_000348.4:c.282-196G>A
MANE Select
|
NP_000339.2:n.282-196G>A
|
|