ENST00000338508.9:c.3213-259G>A
|
ENSP00000345193.7:n.3213-259G>A
|
|
ENST00000412252.6:c.758-259G>A
|
ENSP00000414876.2:n.758-259G>A
|
|
ENST00000601538.6:c.4980-259G>A
MANE Select
|
ENSP00000469689.2:n.4980-259G>A
|
|
ENST00000654939.1:c.2489-259G>A
|
|
|
ENST00000656230.1:c.3843-259G>A
|
ENSP00000499561.1:n.3843-259G>A
|
|
ENST00000659264.1:c.3270-259G>A
|
ENSP00000499270.1:n.3270-259G>A
|
|
ENST00000338508.8:c.3216-259G>A
|
ENSP00000345193.6:n.3216-259G>A
|
|
ENST00000357171.7:c.719-259G>A
|
ENSP00000349694.4:n.719-259G>A
|
|
ENST00000409161.5:c.3192-259G>A
|
ENSP00000386491.1:n.3192-259G>A
|
|
ENST00000412252.5:c.756-259G>A
|
|
|
ENST00000423696.6:c.3843-259G>A
|
ENSP00000394536.2:n.3843-259G>A
|
|
ENST00000424924.5:c.2817-259G>A
|
ENSP00000402944.1:n.2817-259G>A
|
|
ENST00000449833.6:c.3216-259G>A
|
ENSP00000399423.3:n.3216-259G>A
|
|
ENST00000601538.5:c.4980-259G>A
|
ENSP00000469689.2:n.4980-259G>A
|
|
ENST00000606715.3:n.1473G>A
|
|
|
NM_012309.4:c.4980-259G>A
|
NP_036441.2:n.4980-259G>A
|
|
NM_133266.4:c.3216-259G>A
|
NP_573573.2:n.3216-259G>A
|
|
NR_110766.1:n.834-259G>A
|
|
|
XM_005277930.2:c.4980-259G>A
|
XP_005277987.1:n.4980-259G>A
|
|
XM_005277932.2:c.3843-259G>A
|
XP_005277989.1:n.3843-259G>A
|
|
XM_006718478.2:c.4950-259G>A
|
XP_006718541.1:n.4950-259G>A
|
|
XM_011544854.1:c.4992-259G>A
|
XP_011543156.1:n.4992-259G>A
|
|
XM_011544855.1:c.4971-259G>A
|
XP_011543157.1:n.4971-259G>A
|
|
XM_011544856.1:c.4965-259G>A
|
XP_011543158.1:n.4965-259G>A
|
|
XM_011544857.1:c.4944-259G>A
|
XP_011543159.1:n.4944-259G>A
|
|
XM_011544859.1:c.3855-259G>A
|
XP_011543161.1:n.3855-259G>A
|
|
XM_005277932.3:c.3843-259G>A
|
XP_005277989.1:n.3843-259G>A
|
|
XM_017017387.1:c.4980-259G>A
|
XP_016872876.1:n.4980-259G>A
|
|
XM_017017388.1:c.4980-259G>A
|
XP_016872877.1:n.4980-259G>A
|
|
XM_017017389.1:c.4953-259G>A
|
XP_016872878.1:n.4953-259G>A
|
|
XM_017017390.1:c.3270-259G>A
|
XP_016872879.1:n.3270-259G>A
|
|
NM_133266.5:c.3216-259G>A
|
NP_573573.2:n.3216-259G>A
|
|
NR_110766.2:n.835-259G>A
|
|
|
NM_001379226.1:c.3843-259G>A
|
NP_001366155.1:n.3843-259G>A
|
|
NM_012309.5:c.4980-259G>A
MANE Select
|
NP_036441.2:n.4980-259G>A
|
|