ENST00000225927.7:c.708C>T
MANE Select
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ENSP00000225927.1:p.Phe236=
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|
ENST00000225927.6:c.708C>T
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ENSP00000225927.1:p.Phe236=
|
|
ENST00000586516.5:c.310C>T
|
|
|
ENST00000591587.1:c.303C>T
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ENSP00000467836.1:p.Phe101=
|
|
NM_000263.3:c.708C>T
|
NP_000254.2:p.Phe236=
|
|
XM_006721920.2:c.-35C>T
|
XP_006721983.1:n.-35C>T
|
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XM_011524840.1:c.-35C>T
|
XP_011523142.1:n.-35C>T
|
|
XM_017024687.1:c.-35C>T
|
XP_016880176.1:n.-35C>T
|
|
XM_024450771.1:c.765C>T
|
XP_024306539.1:p.Phe255=
|
|
XM_024450772.1:c.-35C>T
|
XP_024306540.1:n.-35C>T
|
|
NM_000263.4:c.708C>T
MANE Select
|
NP_000254.2:p.Phe236=
|
|