ENST00000525748.6:c.1499+254T=
MANE Select
|
ENSP00000434364.2:n.1499+254T=
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|
ENST00000298923.11:c.*796+254T=
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ENSP00000298923.7:n.*796+254T=
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|
ENST00000525748.5:c.1499+254T=
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ENSP00000434364.1:n.1499+254T=
|
|
NM_004211.3:c.1499+254T=
|
NP_004202.2:n.1499+254T=
|
|
XM_005253225.1:c.797+254T=
|
XP_005253282.1:n.797+254T=
|
|
XM_011520473.1:c.1499+254T=
|
XP_011518775.1:n.1499+254T=
|
|
NM_001318369.1:c.797+254T=
|
NP_001305298.1:n.797+254T=
|
|
NM_004211.4:c.1499+254T=
|
NP_004202.3:n.1499+254T=
|
|
XM_017018544.2:c.623+254T=
|
XP_016874033.1:n.623+254T=
|
|
XM_017018545.2:c.458+254T=
|
XP_016874034.1:n.458+254T=
|
|
NM_001318369.2:c.797+254T=
|
NP_001305298.1:n.797+254T=
|
|
NM_004211.5:c.1499+254T=
MANE Select
|
NP_004202.4:n.1499+254T=
|
|