ENST00000225964.10:c.4142C>A
MANE Select
|
ENSP00000225964.6:p.Thr1381Asn
|
|
ENST00000225964.9:c.4142C>A
|
ENSP00000225964.5:p.Thr1381Asn
|
|
ENST00000510710.3:n.1107C>A
|
|
|
NM_000088.3:c.4142C>A , LRG_1t1:c.4142C>A
|
NP_000079.2:p.Thr1381Asn
|
|
XM_005257058.3:c.3872C>A
|
XP_005257115.2:p.Thr1291Asn
|
|
XM_005257059.3:c.3224C>A
|
XP_005257116.2:p.Thr1075Asn
|
|
XM_011524341.1:c.3944C>A
|
XP_011522643.1:p.Thr1315Asn
|
|
XM_005257058.4:c.3872C>A
|
XP_005257115.2:p.Thr1291Asn
|
|
XM_005257059.4:c.3224C>A
|
XP_005257116.2:p.Thr1075Asn
|
|
NM_000088.4:c.4142C>A
MANE Select
|
NP_000079.2:p.Thr1381Asn
|
|