ENST00000461271.6:c.-283G>T
|
ENSP00000464056.2:n.-283G>T
|
|
ENST00000697675.1:n.37G>T
|
|
|
ENST00000697676.1:n.26G>T
|
|
|
ENST00000697677.1:n.24G>T
|
|
|
ENST00000697678.1:n.24G>T
|
|
|
ENST00000697679.1:n.17G>T
|
|
|
ENST00000697680.1:c.-35G>T
|
ENSP00000513392.1:n.-35G>T
|
|
ENST00000697681.1:c.-35G>T
|
ENSP00000513393.1:n.-35G>T
|
|
ENST00000697683.1:c.-35G>T
|
ENSP00000513395.1:n.-35G>T
|
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ENST00000697684.1:n.26G>T
|
|
|
ENST00000697685.1:c.-35G>T
|
ENSP00000513396.1:n.-35G>T
|
|
ENST00000697686.1:c.-230G>T
|
ENSP00000513397.1:n.-230G>T
|
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ENST00000697687.1:n.12G>T
|
|
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ENST00000697688.1:n.12G>T
|
|
|
ENST00000697689.1:c.-35G>T
|
ENSP00000513398.1:n.-35G>T
|
|
ENST00000697690.1:c.-35G>T
|
ENSP00000513399.1:n.-35G>T
|
|
ENST00000337432.9:c.-35G>T
MANE Select
|
ENSP00000336701.4:n.-35G>T
|
|
ENST00000337432.8:c.-35G>T
|
ENSP00000336701.4:n.-35G>T
|
|
ENST00000461271.5:c.-283G>T
|
ENSP00000464056.1:n.-283G>T
|
|
ENST00000475762.5:c.-35G>T
|
ENSP00000432421.1:n.-35G>T
|
|
ENST00000476741.2:n.8G>T
|
|
|
ENST00000486827.1:c.-35G>T
|
ENSP00000436761.1:n.-35G>T
|
|
ENST00000487525.5:c.-35G>T
|
ENSP00000431637.1:n.-35G>T
|
|
ENST00000487921.5:n.34G>T
|
|
|
ENST00000583539.5:c.-35G>T
|
ENSP00000463121.1:n.-35G>T
|
|
NM_002876.3:c.-35G>T
|
NP_002867.1:n.-35G>T
|
|
NM_058216.2:c.-35G>T
|
NP_478123.1:n.-35G>T
|
|
NR_103872.1:n.37G>T
|
|
|
NR_103873.1:n.37G>T
|
|
|
XM_006722001.2:c.-35G>T
|
XP_006722064.1:n.-35G>T
|
|
XM_006722002.2:c.-35G>T
|
XP_006722065.1:n.-35G>T
|
|
XM_006722004.2:c.-283G>T
|
XP_006722067.1:n.-283G>T
|
|
XM_006722005.2:c.-230G>T
|
XP_006722068.1:n.-230G>T
|
|
XM_011525092.1:c.-583G>T
|
XP_011523394.1:n.-583G>T
|
|
XM_011525093.1:c.-744G>T
|
XP_011523395.1:n.-744G>T
|
|
XR_934513.1:n.39G>T
|
|
|
XR_934514.1:n.39G>T
|
|
|
XM_006722001.4:c.-35G>T
|
XP_006722064.1:n.-35G>T
|
|
XM_006722002.4:c.-35G>T
|
XP_006722065.1:n.-35G>T
|
|
XM_006722004.3:c.-283G>T
|
XP_006722067.1:n.-283G>T
|
|
XM_006722005.3:c.-230G>T
|
XP_006722068.1:n.-230G>T
|
|
XM_017024914.1:c.-283G>T
|
XP_016880403.1:n.-283G>T
|
|
XM_017024917.1:c.-230G>T
|
XP_016880406.1:n.-230G>T
|
|
XR_934513.3:n.470G>T
|
|
|
XR_934514.3:n.470G>T
|
|
|
NM_058216.3:c.-35G>T
MANE Select
|
NP_478123.1:n.-35G>T
|
|
NR_103872.2:n.8G>T
|
|
|
NM_002876.4:c.-35G>T
|
NP_002867.1:n.-35G>T
|
|