ENST00000356839.10:c.477+50A>G
MANE Select
|
ENSP00000349297.5:n.477+50A>G
|
|
ENST00000322910.9:c.*432+50A>G
|
ENSP00000325395.5:n.*432+50A>G
|
|
ENST00000350303.9:c.411+50A>G
|
ENSP00000344152.5:n.411+50A>G
|
|
ENST00000356839.9:c.477+50A>G
|
ENSP00000349297.5:n.477+50A>G
|
|
ENST00000543245.6:c.546+50A>G
|
ENSP00000438689.2:n.546+50A>G
|
|
ENST00000577191.5:n.554+50A>G
|
|
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ENST00000577433.5:n.685+50A>G
|
|
|
ENST00000577857.5:n.293+278A>G
|
|
|
ENST00000579286.5:n.658+50A>G
|
|
|
ENST00000579886.2:c.315+50A>G
|
ENSP00000463246.1:n.315+50A>G
|
|
ENST00000580365.1:n.208+50A>G
|
|
|
ENST00000581378.5:c.176+50A>G
|
|
|
ENST00000581562.5:n.524+50A>G
|
|
|
ENST00000582056.5:n.710A>G
|
|
|
ENST00000582166.1:n.458+50A>G
|
|
|
ENST00000583312.5:c.477+50A>G
|
ENSP00000467920.1:n.477+50A>G
|
|
NM_000018.3:c.477+50A>G
|
NP_000009.1:n.477+50A>G
|
|
NM_001033859.2:c.411+50A>G
|
NP_001029031.1:n.411+50A>G
|
|
NM_001270447.1:c.546+50A>G
|
NP_001257376.1:n.546+50A>G
|
|
NM_001270448.1:c.249+50A>G
|
NP_001257377.1:n.249+50A>G
|
|
XM_006721516.2:c.477+50A>G
|
XP_006721579.2:n.477+50A>G
|
|
XM_011523829.1:c.477+50A>G
|
XP_011522131.1:n.477+50A>G
|
|
XM_011523830.1:c.477+50A>G
|
XP_011522132.1:n.477+50A>G
|
|
XR_934021.1:n.584+50A>G
|
|
|
XR_934022.1:n.584+50A>G
|
|
|
XR_934023.1:n.584+50A>G
|
|
|
XM_006721516.3:c.477+50A>G
|
XP_006721579.2:n.477+50A>G
|
|
XM_011523829.2:c.477+50A>G
|
XP_011522131.1:n.477+50A>G
|
|
XM_011523830.2:c.477+50A>G
|
XP_011522132.1:n.477+50A>G
|
|
XM_024450741.1:c.477+50A>G
|
XP_024306509.1:n.477+50A>G
|
|
XR_934021.2:n.536+50A>G
|
|
|
XR_934022.2:n.536+50A>G
|
|
|
XR_934023.2:n.536+50A>G
|
|
|
NM_000018.4:c.477+50A>G
MANE Select
|
NP_000009.1:n.477+50A>G
|
|
NM_001033859.3:c.411+50A>G
|
NP_001029031.1:n.411+50A>G
|
|
NM_001270447.2:c.546+50A>G
|
NP_001257376.1:n.546+50A>G
|
|
NM_001270448.2:c.249+50A>G
|
NP_001257377.1:n.249+50A>G
|
|