ENST00000405460.9:c.9388T>G
MANE Select
|
ENSP00000384582.2:p.Ser3130Ala
|
|
ENST00000639431.1:c.265+40461T>G
|
ENSP00000491057.1:n.265+40461T>G
|
|
ENST00000639473.1:n.4847T>G
|
|
|
ENST00000640012.1:c.3195T>G
|
|
|
ENST00000640374.1:n.2532T>G
|
|
|
ENST00000640779.1:c.4117T>G
|
|
|
ENST00000405460.6:c.9388T>G
|
ENSP00000384582.2:p.Ser3130Ala
|
|
ENST00000509621.1:c.2085T>G
|
|
|
NM_032119.3:c.9388T>G
|
NP_115495.3:p.Ser3130Ala
|
|
NR_003149.1:n.9401T>G
|
|
|
XM_011543675.1:c.9385T>G
|
XP_011541977.1:p.Ser3129Ala
|
|
XM_011543676.1:c.9307T>G
|
XP_011541978.1:p.Ser3103Ala
|
|
XM_011543677.1:c.6691T>G
|
XP_011541979.1:p.Ser2231Ala
|
|
XM_011543678.1:c.9388T>G
|
XP_011541980.1:p.Ser3130Ala
|
|
XM_011543679.1:c.9388T>G
|
XP_011541981.1:p.Ser3130Ala
|
|
XR_948560.1:n.272-861A>C
|
|
|
NM_032119.4:c.9388T>G
MANE Select
|
NP_115495.3:p.Ser3130Ala
|
|
XM_017009963.2:c.9409T>G
|
XP_016865452.1:p.Ser3137Ala
|
|
XM_017009964.2:c.9406T>G
|
XP_016865453.1:p.Ser3136Ala
|
|
XM_017009965.1:c.9406T>G
|
XP_016865454.1:p.Ser3136Ala
|
|
XM_017009966.2:c.9328T>G
|
XP_016865455.1:p.Ser3110Ala
|
|
XM_017009967.1:c.9313T>G
|
XP_016865456.1:p.Ser3105Ala
|
|
XM_017009968.2:c.9409T>G
|
XP_016865457.1:p.Ser3137Ala
|
|
XM_017009969.2:c.9409T>G
|
XP_016865458.1:p.Ser3137Ala
|
|
XM_017009970.2:c.9409T>G
|
XP_016865459.1:p.Ser3137Ala
|
|
XM_017009971.2:c.9409T>G
|
XP_016865460.1:p.Ser3137Ala
|
|
XM_017009972.1:c.2527T>G
|
XP_016865461.1:p.Ser843Ala
|
|
XM_017009973.1:c.2506T>G
|
XP_016865462.1:p.Ser836Ala
|
|
XM_017009974.2:c.9409T>G
|
XP_016865463.1:p.Ser3137Ala
|
|
XR_001742802.1:n.2523-861A>C
|
|
|
NR_003149.2:n.9404T>G
|
|
|