ENST00000405460.9:c.10963G>T
MANE Select
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ENSP00000384582.2:p.Ala3655Ser
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ENST00000425867.3:c.94G>T
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ENSP00000392618.3:p.Ala32Ser
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ENST00000639431.1:c.265+69575G>T
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ENSP00000491057.1:n.265+69575G>T
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ENST00000640374.1:n.4107G>T
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ENST00000640464.1:n.1382G>T
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ENST00000405460.6:c.10963G>T
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ENSP00000384582.2:p.Ala3655Ser
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ENST00000509621.1:c.3660G>T
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NM_032119.3:c.10963G>T
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NP_115495.3:p.Ala3655Ser
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NR_003149.1:n.10976G>T
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XM_011543675.1:c.10960G>T
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XP_011541977.1:p.Ala3654Ser
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XM_011543676.1:c.10882G>T
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XP_011541978.1:p.Ala3628Ser
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XM_011543677.1:c.8266G>T
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XP_011541979.1:p.Ala2756Ser
|
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XM_011543678.1:c.10963G>T
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XP_011541980.1:p.Ala3655Ser
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NM_032119.4:c.10963G>T
MANE Select
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NP_115495.3:p.Ala3655Ser
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XM_017009963.2:c.10984G>T
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XP_016865452.1:p.Ala3662Ser
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XM_017009964.2:c.10981G>T
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XP_016865453.1:p.Ala3661Ser
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XM_017009965.1:c.10981G>T
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XP_016865454.1:p.Ala3661Ser
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XM_017009966.2:c.10903G>T
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XP_016865455.1:p.Ala3635Ser
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XM_017009967.1:c.10888G>T
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XP_016865456.1:p.Ala3630Ser
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XM_017009968.2:c.10984G>T
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XP_016865457.1:p.Ala3662Ser
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XM_017009969.2:c.10984G>T
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XP_016865458.1:p.Ala3662Ser
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XM_017009970.2:c.10984G>T
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XP_016865459.1:p.Ala3662Ser
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XM_017009971.2:c.10984G>T
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XP_016865460.1:p.Ala3662Ser
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XM_017009972.1:c.4102G>T
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XP_016865461.1:p.Ala1368Ser
|
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XM_017009973.1:c.4081G>T
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XP_016865462.1:p.Ala1361Ser
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NR_003149.2:n.10979G>T
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