ENST00000225964.10:c.3198T>G
MANE Select
|
ENSP00000225964.6:p.Arg1066=
|
|
ENST00000225964.9:c.3198T>G
|
ENSP00000225964.5:p.Arg1066=
|
|
ENST00000486572.1:n.16T>G
|
|
|
ENST00000511732.1:n.142T>G
|
|
|
NM_000088.3:c.3198T>G , LRG_1t1:c.3198T>G
|
NP_000079.2:p.Arg1066=
|
|
XM_005257058.3:c.2928T>G
|
XP_005257115.2:p.Arg976=
|
|
XM_005257059.3:c.2280T>G
|
XP_005257116.2:p.Arg760=
|
|
XM_011524341.1:c.3000T>G
|
XP_011522643.1:p.Arg1000=
|
|
XM_005257058.4:c.2928T>G
|
XP_005257115.2:p.Arg976=
|
|
XM_005257059.4:c.2280T>G
|
XP_005257116.2:p.Arg760=
|
|
NM_000088.4:c.3198T>G
MANE Select
|
NP_000079.2:p.Arg1066=
|
|