ENST00000266771.10:c.769T>C
MANE Select
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ENSP00000266771.5:p.Phe257Leu
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ENST00000266771.9:c.769T>C
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ENSP00000266771.5:p.Phe257Leu
|
|
ENST00000366292.6:n.1081T>C
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|
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ENST00000376740.8:c.348T>C
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|
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ENST00000376744.8:c.605T>C
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|
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ENST00000539703.1:n.419T>C
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|
|
ENST00000614634.1:c.-74T>C
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ENSP00000483143.1:n.-74T>C
|
|
NM_145648.3:c.769T>C
|
NP_663623.1:p.Phe257Leu
|
|
XM_011537895.1:c.919T>C
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XP_011536197.1:p.Phe307Leu
|
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XR_429081.2:n.792T>C
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|
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XR_944494.1:n.942T>C
|
|
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XR_944495.1:n.942T>C
|
|
|
XR_944496.1:n.942T>C
|
|
|
XR_944497.1:n.942T>C
|
|
|
XM_017018791.1:c.919T>C
|
XP_016874280.1:p.Phe307Leu
|
|
XM_017018792.1:c.919T>C
|
XP_016874281.1:p.Phe307Leu
|
|
XM_017018793.1:c.769T>C
|
XP_016874282.1:p.Phe257Leu
|
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XR_002957287.1:n.792T>C
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|
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XR_944496.2:n.942T>C
|
|
|
NM_145648.4:c.769T>C
MANE Select
|
NP_663623.1:p.Phe257Leu
|
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