ENST00000405460.9:c.16321A>C
MANE Select
|
ENSP00000384582.2:p.Met5441Leu
|
|
ENST00000425867.3:c.5275A>C
|
ENSP00000392618.3:p.Met1759Leu
|
|
ENST00000638510.1:n.3588A>C
|
|
|
ENST00000639431.1:c.265+147340A>C
|
ENSP00000491057.1:n.265+147340A>C
|
|
ENST00000640061.1:n.128+1367A>C
|
|
|
ENST00000640407.1:c.2731A>C
|
ENSP00000491425.1:p.Met911Leu
|
|
ENST00000405460.6:c.16321A>C
|
ENSP00000384582.2:p.Met5441Leu
|
|
ENST00000425867.2:c.3304A>C
|
ENSP00000392618.2:p.Met1102Leu
|
|
NM_032119.3:c.16321A>C
|
NP_115495.3:p.Met5441Leu
|
|
NR_003149.1:n.16334A>C
|
|
|
XM_011543675.1:c.16318A>C
|
XP_011541977.1:p.Met5440Leu
|
|
XM_011543676.1:c.16240A>C
|
XP_011541978.1:p.Met5414Leu
|
|
XM_011543677.1:c.13624A>C
|
XP_011541979.1:p.Met4542Leu
|
|
NM_032119.4:c.16321A>C
MANE Select
|
NP_115495.3:p.Met5441Leu
|
|
XM_017009963.2:c.16342A>C
|
XP_016865452.1:p.Met5448Leu
|
|
XM_017009964.2:c.16339A>C
|
XP_016865453.1:p.Met5447Leu
|
|
XM_017009965.1:c.16339A>C
|
XP_016865454.1:p.Met5447Leu
|
|
XM_017009966.2:c.16261A>C
|
XP_016865455.1:p.Met5421Leu
|
|
XM_017009967.1:c.16246A>C
|
XP_016865456.1:p.Met5416Leu
|
|
XM_017009968.2:c.16162A>C
|
XP_016865457.1:p.Met5388Leu
|
|
XM_017009969.2:c.16342A>C
|
XP_016865458.1:p.Met5448Leu
|
|
XM_017009972.1:c.9460A>C
|
XP_016865461.1:p.Met3154Leu
|
|
XM_017009973.1:c.9439A>C
|
XP_016865462.1:p.Met3147Leu
|
|
NR_003149.2:n.16337A>C
|
|
|