ENST00000225964.10:c.1416A>C
MANE Select
|
ENSP00000225964.6:p.Arg472=
|
|
ENST00000225964.9:c.1416A>C
|
ENSP00000225964.5:p.Arg472=
|
|
ENST00000471344.1:n.360A>C
|
|
|
NM_000088.3:c.1416A>C , LRG_1t1:c.1416A>C
|
NP_000079.2:p.Arg472=
|
|
XM_005257058.3:c.1416A>C
|
XP_005257115.2:p.Arg472=
|
|
XM_005257059.3:c.957+1548A>C
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XP_005257116.2:n.957+1548A>C
|
|
XM_011524341.1:c.1218A>C
|
XP_011522643.1:p.Arg406=
|
|
XM_005257058.4:c.1416A>C
|
XP_005257115.2:p.Arg472=
|
|
XM_005257059.4:c.957+1548A>C
|
XP_005257116.2:n.957+1548A>C
|
|
NM_000088.4:c.1416A>C
MANE Select
|
NP_000079.2:p.Arg472=
|
|