|
ENST00000421709.2:c.197C>T
|
ENSP00000388120.2:p.Thr66Met
|
|
|
ENST00000700228.1:c.257C>T
|
ENSP00000514865.1:p.Thr86Met
|
|
|
ENST00000700231.1:c.386C>T
|
ENSP00000514868.1:p.Thr129Met
|
|
|
ENST00000339562.9:c.386C>T
MANE Select
|
ENSP00000344479.4:p.Thr129Met
|
|
|
ENST00000675870.1:c.197C>T
|
ENSP00000502739.1:p.Thr66Met
|
|
|
ENST00000339562.8:c.386C>T
|
ENSP00000344479.4:p.Thr129Met
|
|
|
ENST00000406048.2:c.208+113C>T
|
|
|
|
ENST00000409108.6:c.386C>T
|
ENSP00000386993.2:p.Thr129Met
|
|
|
ENST00000409572.5:c.386C>T
|
ENSP00000386747.1:p.Thr129Met
|
|
|
ENST00000417764.5:c.197C>T
|
ENSP00000415632.1:p.Thr66Met
|
|
|
ENST00000417972.5:c.197C>T
|
ENSP00000394671.1:p.Thr66Met
|
|
|
ENST00000421709.1:c.197C>T
|
ENSP00000388120.1:p.Thr66Met
|
|
|
ENST00000424077.1:c.386C>T
|
ENSP00000406808.1:p.Thr129Met
|
|
|
ENST00000426264.5:c.197C>T
|
ENSP00000389986.1:p.Thr66Met
|
|
|
ENST00000429376.5:c.197C>T
|
ENSP00000410952.1:p.Thr66Met
|
|
|
NM_006186.3:c.386C>T
|
NP_006177.1:p.Thr129Met
|
|
|
XM_005246621.2:c.419C>T
|
XP_005246678.1:p.Thr140Met
|
|
|
XM_005246622.2:c.197C>T
|
XP_005246679.1:p.Thr66Met
|
|
|
XM_005246623.1:c.197C>T
|
XP_005246680.1:p.Thr66Met
|
|
|
XM_006712553.2:c.419C>T
|
XP_006712616.1:p.Thr140Met
|
|
|
XM_011511246.1:c.419C>T
|
XP_011509548.1:p.Thr140Met
|
|
|
XR_427087.2:n.2592C>T
|
|
|
|
NM_173173.2:c.197C>T
|
NP_775265.1:p.Thr66Met
|
|
|
XM_005246621.4:c.419C>T
|
XP_005246678.1:p.Thr140Met
|
|
|
XM_006712553.4:c.419C>T
|
XP_006712616.1:p.Thr140Met
|
|
|
XM_011511246.2:c.419C>T
|
XP_011509548.1:p.Thr140Met
|
|
|
XM_017004219.2:c.386C>T
|
XP_016859708.1:p.Thr129Met
|
|
|
XM_017004220.2:c.386C>T
|
XP_016859709.1:p.Thr129Met
|
|
|
XR_001738751.2:n.754C>T
|
|
|
|
XR_001738752.2:n.576C>T
|
|
|
|
XR_427087.4:n.633C>T
|
|
|
|
NM_006186.4:c.386C>T
MANE Select
|
NP_006177.1:p.Thr129Met
|
|
|
NM_173173.3:c.197C>T
|
NP_775265.1:p.Thr66Met
|
|
