|
NM_032119.4:c.17645A>G
MANE Select
|
NP_115495.3:p.Tyr5882Cys
|
|
ENST00000405460.9:c.17645A>G
MANE Select
|
ENSP00000384582.2:p.Tyr5882Cys
|
|
NM_032119.3:c.17645A>G
|
NP_115495.3:p.Tyr5882Cys
|
|
NR_003149.1:n.17658A>G
|
|
|
NR_003149.2:n.17661A>G
|
|
|
ENST00000405460.6:c.17645A>G
|
ENSP00000384582.2:p.Tyr5882Cys
|
|
ENST00000425867.2:c.4628A>G
|
ENSP00000392618.2:p.Tyr1543Cys
|
|
ENST00000425867.3:c.6599A>G
|
ENSP00000392618.3:p.Tyr2200Cys
|
|
ENST00000503852.1:n.193A>G
|
|
|
ENST00000638510.1:n.4912A>G
|
|
|
ENST00000638990.1:c.857A>G
|
|
|
ENST00000639431.1:c.266-129553A>G
|
ENSP00000491057.1:n.266-129553A>G
|
|
ENST00000640407.1:c.4094A>G
|
ENSP00000491425.1:n.4094A>G
|
|
XM_011543675.1:c.17642A>G
|
XP_011541977.1:p.Tyr5881Cys
|
|
XM_011543676.1:c.17564A>G
|
XP_011541978.1:p.Tyr5855Cys
|
|
XM_011543677.1:c.14948A>G
|
XP_011541979.1:p.Tyr4983Cys
|
|
XM_017009963.2:c.17666A>G
|
XP_016865452.1:p.Tyr5889Cys
|
|
XM_017009964.2:c.17663A>G
|
XP_016865453.1:p.Tyr5888Cys
|
|
XM_017009965.1:c.17663A>G
|
XP_016865454.1:p.Tyr5888Cys
|
|
XM_017009966.2:c.17585A>G
|
XP_016865455.1:p.Tyr5862Cys
|
|
XM_017009967.1:c.17570A>G
|
XP_016865456.1:p.Tyr5857Cys
|
|
XM_017009968.2:c.17486A>G
|
XP_016865457.1:p.Tyr5829Cys
|
|
XM_017009969.2:c.17666A>G
|
XP_016865458.1:p.Tyr5889Cys
|
|
XM_017009972.1:c.10784A>G
|
XP_016865461.1:p.Tyr3595Cys
|
|
XM_017009973.1:c.10763A>G
|
XP_016865462.1:p.Tyr3588Cys
|