|
ENST00000647720.2:c.3214C>T
|
ENSP00000497673.2:p.Pro1072Ser
|
|
|
ENST00000647978.2:c.*2928C>T
|
ENSP00000497658.1:n.*2928C>T
|
|
|
ENST00000649781.2:c.3031C>T
|
ENSP00000497203.1:p.Pro1011Ser
|
|
|
ENST00000685018.2:c.3214C>T
|
ENSP00000510194.2:p.Pro1072Ser
|
|
|
ENST00000687278.2:c.3214C>T
|
ENSP00000509593.2:p.Pro1072Ser
|
|
|
ENST00000699585.1:c.3214C>T
|
ENSP00000514456.1:p.Pro1072Ser
|
|
|
ENST00000699598.1:c.3214C>T
|
ENSP00000514467.1:p.Pro1072Ser
|
|
|
ENST00000699599.1:c.3214C>T
|
ENSP00000514468.1:p.Pro1072Ser
|
|
|
ENST00000699600.1:c.3214C>T
|
ENSP00000514469.1:p.Pro1072Ser
|
|
|
ENST00000699601.1:c.*1514C>T
|
ENSP00000514470.1:n.*1514C>T
|
|
|
ENST00000699602.1:c.3214C>T
|
ENSP00000514471.1:p.Pro1072Ser
|
|
|
ENST00000699604.1:c.*3038C>T
|
ENSP00000514472.1:n.*3038C>T
|
|
|
ENST00000699605.1:c.2788C>T
|
ENSP00000514473.1:p.Pro930Ser
|
|
|
ENST00000687278.1:c.805C>T
|
ENSP00000509593.1:p.Pro269Ser
|
|
|
ENST00000003084.11:c.3214C>T
MANE Select
|
ENSP00000003084.6:p.Pro1072Ser
|
|
|
ENST00000647720.1:c.864C>T
|
|
|
|
ENST00000648260.1:c.1996C>T
|
ENSP00000497957.1:p.Pro666Ser
|
|
|
ENST00000649406.1:c.3031C>T
|
ENSP00000497965.1:p.Pro1011Ser
|
|
|
ENST00000649781.1:c.3031C>T
|
ENSP00000497203.1:p.Pro1011Ser
|
|
|
ENST00000003084.10:c.3214C>T
|
ENSP00000003084.6:p.Pro1072Ser
|
|
|
ENST00000426809.5:c.3124C>T
|
ENSP00000389119.1:p.Pro1042Ser
|
|
|
ENST00000468795.1:c.39C>T
|
|
|
|
NM_000492.3:c.3214C>T , LRG_663t1:c.3214C>T
|
NP_000483.3:p.Pro1072Ser
|
|
|
XM_011515751.1:c.3304C>T
|
XP_011514053.1:p.Pro1102Ser
|
|
|
XM_011515752.1:c.3304C>T
|
XP_011514054.1:p.Pro1102Ser
|
|
|
XM_011515753.1:c.2971C>T
|
XP_011514055.1:p.Pro991Ser
|
|
|
XM_011515754.1:c.2971C>T
|
XP_011514056.1:p.Pro991Ser
|
|
|
NM_000492.4:c.3214C>T
MANE Select
|
NP_000483.3:p.Pro1072Ser
|
|
