ENST00000405460.9:c.15647T>G
MANE Select
|
ENSP00000384582.2:p.Ile5216Ser
|
|
ENST00000425867.3:c.4601T>G
|
ENSP00000392618.3:p.Ile1534Ser
|
|
ENST00000638510.1:n.2914T>G
|
|
|
ENST00000639431.1:c.265+134698T>G
|
ENSP00000491057.1:n.265+134698T>G
|
|
ENST00000640407.1:c.2057T>G
|
ENSP00000491425.1:p.Ile686Ser
|
|
ENST00000405460.6:c.15647T>G
|
ENSP00000384582.2:p.Ile5216Ser
|
|
ENST00000425867.2:c.2630T>G
|
ENSP00000392618.2:p.Ile877Ser
|
|
NM_032119.3:c.15647T>G
|
NP_115495.3:p.Ile5216Ser
|
|
NR_003149.1:n.15660T>G
|
|
|
XM_011543675.1:c.15644T>G
|
XP_011541977.1:p.Ile5215Ser
|
|
XM_011543676.1:c.15566T>G
|
XP_011541978.1:p.Ile5189Ser
|
|
XM_011543677.1:c.12950T>G
|
XP_011541979.1:p.Ile4317Ser
|
|
NM_032119.4:c.15647T>G
MANE Select
|
NP_115495.3:p.Ile5216Ser
|
|
XM_017009963.2:c.15668T>G
|
XP_016865452.1:p.Ile5223Ser
|
|
XM_017009964.2:c.15665T>G
|
XP_016865453.1:p.Ile5222Ser
|
|
XM_017009965.1:c.15665T>G
|
XP_016865454.1:p.Ile5222Ser
|
|
XM_017009966.2:c.15587T>G
|
XP_016865455.1:p.Ile5196Ser
|
|
XM_017009967.1:c.15572T>G
|
XP_016865456.1:p.Ile5191Ser
|
|
XM_017009968.2:c.15488T>G
|
XP_016865457.1:p.Ile5163Ser
|
|
XM_017009969.2:c.15668T>G
|
XP_016865458.1:p.Ile5223Ser
|
|
XM_017009972.1:c.8786T>G
|
XP_016865461.1:p.Ile2929Ser
|
|
XM_017009973.1:c.8765T>G
|
XP_016865462.1:p.Ile2922Ser
|
|
NR_003149.2:n.15663T>G
|
|
|