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ENST00000600128.6:c.7950C>T
(FBN3)
MANE Select
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ENSP00000470498.1:p.Ser2650=
|
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ENST00000651877.1:c.8076C>T
(FBN3)
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ENSP00000498507.1:p.Ser2692=
|
|
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ENST00000270509.6:c.7950C>T
(FBN3)
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ENSP00000270509.2:p.Ser2650=
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ENST00000351593.9:c.-20+77118C>T
(ELAVL1)
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ENSP00000264073.6:n.-20+77118C>T
|
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ENST00000600128.5:c.7950C>T
(FBN3)
|
ENSP00000470498.1:p.Ser2650=
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|
ENST00000601739.5:c.7950C>T
(FBN3)
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ENSP00000472324.1:p.Ser2650=
|
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NM_032447.3:c.7950C>T
(FBN3)
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NP_115823.3:p.Ser2650=
|
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XM_011528373.1:c.7950C>T
(FBN3)
|
XP_011526675.1:p.Ser2650=
|
|
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NM_001321431.1:c.7950C>T
(FBN3)
|
NP_001308360.1:p.Ser2650=
|
|
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NM_032447.4:c.7950C>T
(FBN3)
|
NP_115823.3:p.Ser2650=
|
|
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XM_017027372.1:c.7950C>T
(FBN3)
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XP_016882861.1:p.Ser2650=
|
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XM_017027373.1:c.7890C>T
(FBN3)
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XP_016882862.1:p.Ser2630=
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XM_017027374.2:c.7854C>T
(FBN3)
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XP_016882863.1:p.Ser2618=
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XM_017027375.2:c.7827C>T
(FBN3)
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XP_016882864.1:p.Ser2609=
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XM_017027376.1:c.7821C>T
(FBN3)
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XP_016882865.1:p.Ser2607=
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XM_017027377.2:c.5367C>T
(FBN3)
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XP_016882866.1:p.Ser1789=
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XM_017027378.2:c.4308C>T
(FBN3)
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XP_016882867.1:p.Ser1436=
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XM_017027379.1:c.8076C>T
(FBN3)
|
XP_016882868.1:p.Ser2692=
|
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|
NM_032447.5:c.7950C>T
(FBN3)
MANE Select
|
NP_115823.3:p.Ser2650=
|
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|
NM_001321431.2:c.7950C>T
(FBN3)
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NP_001308360.1:p.Ser2650=
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