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ENSP00000355746.2:p.Ile425=
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ENST00000366783.8:c.1273A=
MANE Select
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ENSP00000355747.3:p.Ile425=
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ENST00000471728.2:n.1911A=
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ENST00000524196.6:c.1273A=
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ENST00000677748.1:n.3528A=
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|
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|
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|
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|
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|
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|
|
|
NM_000447.2:c.1273A=
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|
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NM_012486.2:c.1270A=
|
NP_036618.2:p.Ile424=
|
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XM_005273199.2:c.1273A=
|
XP_005273256.1:p.Ile425=
|
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XM_011544236.1:c.841A=
|
XP_011542538.1:p.Ile281=
|
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XR_949149.1:n.2007A=
|
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XM_005273199.4:c.1273A=
|
XP_005273256.1:p.Ile425=
|
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XM_017001835.1:c.1273A=
|
XP_016857324.1:p.Ile425=
|
|
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XM_017001836.1:c.1270A=
|
XP_016857325.1:p.Ile424=
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XR_001737316.2:n.1478-2215A=
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XR_001737317.2:n.1478-2215A=
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XR_001737318.2:n.1988A=
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XR_001737319.1:n.2331A=
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XR_001737320.1:n.2328A=
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XR_001737321.1:n.1823A=
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XR_949149.2:n.1985A=
|
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XR_949150.3:n.2204A=
|
|
|
|
NM_000447.3:c.1273A=
MANE Select
|
NP_000438.2:p.Ile425=
|
|
|
NM_012486.3:c.1270A=
|
NP_036618.2:p.Ile424=
|
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