ENST00000298229.7:c.182+218A>G
MANE Select
|
ENSP00000298229.2:n.182+218A>G
|
|
ENST00000298229.6:c.182+218A>G
|
ENSP00000298229.2:n.182+218A>G
|
|
ENST00000541544.1:n.98+218A>G
|
|
|
NM_001567.3:c.182+218A>G
|
NP_001558.3:n.182+218A>G
|
|
XM_005273978.3:c.182+218A>G
|
XP_005274035.1:n.182+218A>G
|
|
XM_005273979.3:c.182+218A>G
|
XP_005274036.1:n.182+218A>G
|
|
XM_011544999.1:c.182+218A>G
|
XP_011543301.1:n.182+218A>G
|
|
XM_011545000.1:c.182+218A>G
|
XP_011543302.1:n.182+218A>G
|
|
XM_005273979.4:c.182+218A>G
|
XP_005274036.1:n.182+218A>G
|
|
XM_011544999.2:c.182+218A>G
|
XP_011543301.1:n.182+218A>G
|
|
XM_024448501.1:c.182+218A>G
|
XP_024304269.1:n.182+218A>G
|
|
XM_024448502.1:c.182+218A>G
|
XP_024304270.1:n.182+218A>G
|
|
XM_024448503.1:c.62-66A>G
|
XP_024304271.1:n.62-66A>G
|
|
XM_024448504.1:c.182+218A>G
|
XP_024304272.1:n.182+218A>G
|
|
XM_024448505.1:c.182+218A>G
|
XP_024304273.1:n.182+218A>G
|
|
NM_001567.4:c.182+218A>G
MANE Select
|
NP_001558.3:n.182+218A>G
|
|