ENST00000449606.7:c.819C>G
MANE Select
|
ENSP00000395196.2:p.His273Gln
|
|
ENST00000674054.1:c.819C>G
|
ENSP00000501251.1:p.His273Gln
|
|
ENST00000449606.5:c.819C>G
|
ENSP00000395196.1:p.His273Gln
|
|
ENST00000562402.1:n.423C>G
|
|
|
ENST00000563232.1:c.819C>G
|
ENSP00000456218.1:p.His273Gln
|
|
ENST00000563459.5:c.819C>G
|
ENSP00000456467.1:p.His273Gln
|
|
ENST00000564501.5:c.819C>G
|
ENSP00000457107.1:p.His273Gln
|
|
ENST00000564987.1:n.443C>G
|
|
|
ENST00000565344.1:n.192C>G
|
|
|
NM_001083614.1:c.819C>G
|
NP_001077083.1:p.His273Gln
|
|
NM_001308211.1:c.819C>G
|
NP_001295140.1:p.His273Gln
|
|
NR_003501.1:n.851C>G
|
|
|
XM_011545738.1:c.747C>G
|
XP_011544040.1:p.His249Gln
|
|
XM_011545739.1:c.540C>G
|
XP_011544041.1:p.His180Gln
|
|
XR_001751841.1:n.1141C>G
|
|
|
NM_001083614.2:c.819C>G
MANE Select
|
NP_001077083.1:p.His273Gln
|
|
NR_003501.2:n.826C>G
|
|
|