|
NM_032119.4:c.17669T>A
MANE Select
|
NP_115495.3:p.Met5890Lys
|
|
ENST00000405460.9:c.17669T>A
MANE Select
|
ENSP00000384582.2:p.Met5890Lys
|
|
NM_032119.3:c.17669T>A
|
NP_115495.3:p.Met5890Lys
|
|
NR_003149.1:n.17682T>A
|
|
|
NR_003149.2:n.17685T>A
|
|
|
ENST00000405460.6:c.17669T>A
|
ENSP00000384582.2:p.Met5890Lys
|
|
ENST00000425867.2:c.4652T>A
|
ENSP00000392618.2:p.Met1551Lys
|
|
ENST00000425867.3:c.6623T>A
|
ENSP00000392618.3:p.Met2208Lys
|
|
ENST00000503852.1:n.217T>A
|
|
|
ENST00000638510.1:n.4936T>A
|
|
|
ENST00000638990.1:c.881T>A
|
|
|
ENST00000639431.1:c.266-129529T>A
|
ENSP00000491057.1:n.266-129529T>A
|
|
ENST00000640407.1:c.4118T>A
|
ENSP00000491425.1:n.4118T>A
|
|
XM_011543675.1:c.17666T>A
|
XP_011541977.1:p.Met5889Lys
|
|
XM_011543676.1:c.17588T>A
|
XP_011541978.1:p.Met5863Lys
|
|
XM_011543677.1:c.14972T>A
|
XP_011541979.1:p.Met4991Lys
|
|
XM_017009963.2:c.17690T>A
|
XP_016865452.1:p.Met5897Lys
|
|
XM_017009964.2:c.17687T>A
|
XP_016865453.1:p.Met5896Lys
|
|
XM_017009965.1:c.17687T>A
|
XP_016865454.1:p.Met5896Lys
|
|
XM_017009966.2:c.17609T>A
|
XP_016865455.1:p.Met5870Lys
|
|
XM_017009967.1:c.17594T>A
|
XP_016865456.1:p.Met5865Lys
|
|
XM_017009968.2:c.17510T>A
|
XP_016865457.1:p.Met5837Lys
|
|
XM_017009969.2:c.17690T>A
|
XP_016865458.1:p.Met5897Lys
|
|
XM_017009972.1:c.10808T>A
|
XP_016865461.1:p.Met3603Lys
|
|
XM_017009973.1:c.10787T>A
|
XP_016865462.1:p.Met3596Lys
|