|
NM_006736.6:c.783C>T
MANE Select
|
NP_006727.2:p.Tyr261=
|
|
ENST00000336576.10:c.783C>T
MANE Select
|
ENSP00000338019.5:p.Tyr261=
|
|
NM_001039550.1:c.783C>T
|
NP_001034639.1:p.Tyr261=
|
|
NM_001039550.2:c.783C>T
|
NP_001034639.1:p.Tyr261=
|
|
NM_006736.5:c.783C>T
|
NP_006727.2:p.Tyr261=
|
|
ENST00000336576.9:c.783C>T
|
ENSP00000338019.5:p.Tyr261=
|
|
ENST00000392086.8:c.783C>T
|
ENSP00000375936.4:p.Tyr261=
|
|
ENST00000392087.6:c.690C>T
|
ENSP00000375937.2:p.Tyr230=
|
|
ENST00000463463.5:n.774C>T
|
|
|
ENST00000472019.5:n.526C>T
|
|
|
ENST00000473750.5:n.570C>T
|
|
|
ENST00000476254.1:n.407C>T
|
|
|
ENST00000477917.5:n.2387C>T
|
|
|
ENST00000684599.1:n.990C>T
|
|