ENST00000348931.9:c.417A>G
MANE Select
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ENSP00000335384.5:p.Glu139=
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ENST00000348931.8:c.417A>G
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ENSP00000335384.5:p.Glu139=
|
|
ENST00000377940.3:c.351A>G
|
ENSP00000367174.3:p.Glu117=
|
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ENST00000583811.5:c.63A>G
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ENSP00000462463.1:p.Glu21=
|
|
ENST00000584588.5:c.406+655A>G
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ENSP00000462067.1:n.406+655A>G
|
|
NM_198844.2:c.351A>G
|
NP_942141.2:p.Glu117=
|
|
NM_199321.2:c.417A>G
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NP_955353.1:p.Glu139=
|
|
XM_011524298.1:c.417A>G
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XP_011522600.1:p.Glu139=
|
|
XR_002957959.1:n.608A>G
|
|
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NM_198844.3:c.351A>G
|
NP_942141.2:p.Glu117=
|
|
NM_199321.3:c.417A>G
MANE Select
|
NP_955353.1:p.Glu139=
|
|