ENST00000405460.9:c.16315T>A
MANE Select
|
ENSP00000384582.2:p.Cys5439Ser
|
|
ENST00000425867.3:c.5269T>A
|
ENSP00000392618.3:p.Cys1757Ser
|
|
ENST00000638510.1:n.3582T>A
|
|
|
ENST00000639431.1:c.265+147334T>A
|
ENSP00000491057.1:n.265+147334T>A
|
|
ENST00000640061.1:n.128+1361T>A
|
|
|
ENST00000640407.1:c.2725T>A
|
ENSP00000491425.1:p.Cys909Ser
|
|
ENST00000405460.6:c.16315T>A
|
ENSP00000384582.2:p.Cys5439Ser
|
|
ENST00000425867.2:c.3298T>A
|
ENSP00000392618.2:p.Cys1100Ser
|
|
NM_032119.3:c.16315T>A
|
NP_115495.3:p.Cys5439Ser
|
|
NR_003149.1:n.16328T>A
|
|
|
XM_011543675.1:c.16312T>A
|
XP_011541977.1:p.Cys5438Ser
|
|
XM_011543676.1:c.16234T>A
|
XP_011541978.1:p.Cys5412Ser
|
|
XM_011543677.1:c.13618T>A
|
XP_011541979.1:p.Cys4540Ser
|
|
NM_032119.4:c.16315T>A
MANE Select
|
NP_115495.3:p.Cys5439Ser
|
|
XM_017009963.2:c.16336T>A
|
XP_016865452.1:p.Cys5446Ser
|
|
XM_017009964.2:c.16333T>A
|
XP_016865453.1:p.Cys5445Ser
|
|
XM_017009965.1:c.16333T>A
|
XP_016865454.1:p.Cys5445Ser
|
|
XM_017009966.2:c.16255T>A
|
XP_016865455.1:p.Cys5419Ser
|
|
XM_017009967.1:c.16240T>A
|
XP_016865456.1:p.Cys5414Ser
|
|
XM_017009968.2:c.16156T>A
|
XP_016865457.1:p.Cys5386Ser
|
|
XM_017009969.2:c.16336T>A
|
XP_016865458.1:p.Cys5446Ser
|
|
XM_017009972.1:c.9454T>A
|
XP_016865461.1:p.Cys3152Ser
|
|
XM_017009973.1:c.9433T>A
|
XP_016865462.1:p.Cys3145Ser
|
|
NR_003149.2:n.16331T>A
|
|
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