ENST00000340855.11:c.936C>T
MANE Select
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ENSP00000339801.6:p.Gly312=
|
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ENST00000651111.1:c.303C>T
|
ENSP00000498395.1:p.Gly101=
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ENST00000340855.10:c.936C>T
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ENSP00000339801.6:p.Gly312=
|
|
ENST00000370441.8:c.936C>T
|
ENSP00000359470.4:p.Gly312=
|
|
ENST00000422081.6:c.303C>T
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ENSP00000477056.1:p.Gly101=
|
|
ENST00000441880.1:n.114-3286C>T
|
|
|
ENST00000464251.5:c.862C>T
|
ENSP00000428980.1:n.862C>T
|
|
ENST00000466323.5:c.*127C>T
|
ENSP00000418264.1:n.*127C>T
|
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ENST00000490775.5:n.721C>T
|
|
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NM_000202.6:c.936C>T
|
NP_000193.1:p.Gly312=
|
|
NM_001166550.2:c.666C>T
|
NP_001160022.1:p.Gly222=
|
|
NM_006123.4:c.936C>T
|
NP_006114.1:p.Gly312=
|
|
NR_104128.1:n.1283C>T
|
|
|
NM_000202.7:c.936C>T
|
NP_000193.1:p.Gly312=
|
|
NM_001166550.3:c.666C>T
|
NP_001160022.1:p.Gly222=
|
|
NM_000202.8:c.936C>T
MANE Select
|
NP_000193.1:p.Gly312=
|
|
NM_001166550.4:c.666C>T
|
NP_001160022.1:p.Gly222=
|
|
NM_006123.5:c.936C>T
|
NP_006114.1:p.Gly312=
|
|
NR_104128.2:n.1235C>T
|
|
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