ENST00000225964.10:c.862G>T
MANE Select
|
ENSP00000225964.6:p.Glu288Ter
|
|
ENST00000225964.9:c.862G>T
|
ENSP00000225964.5:p.Glu288Ter
|
|
ENST00000485870.1:n.71G>T
|
|
|
ENST00000495677.1:n.589G>T
|
|
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NM_000088.3:c.862G>T , LRG_1t1:c.862G>T
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NP_000079.2:p.Glu288Ter
|
|
XM_005257058.3:c.862G>T
|
XP_005257115.2:p.Glu288Ter
|
|
XM_005257059.3:c.862G>T
|
XP_005257116.2:p.Glu288Ter
|
|
XM_011524341.1:c.862G>T
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XP_011522643.1:p.Glu288Ter
|
|
XM_005257058.4:c.862G>T
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XP_005257115.2:p.Glu288Ter
|
|
XM_005257059.4:c.862G>T
|
XP_005257116.2:p.Glu288Ter
|
|
NM_000088.4:c.862G>T
MANE Select
|
NP_000079.2:p.Glu288Ter
|
|