ENST00000438166.7:c.1928T>G
MANE Select
|
ENSP00000409708.2:p.Ile643Ser
|
|
ENST00000310454.10:c.1928T>G
|
ENSP00000308610.5:p.Ile643Ser
|
|
ENST00000409125.8:c.1550T>G
|
ENSP00000386484.5:p.Ile517Ser
|
|
ENST00000409674.5:c.1928T>G
|
ENSP00000386425.1:p.Ile643Ser
|
|
ENST00000409861.5:c.1928T>G
|
ENSP00000386626.1:p.Ile643Ser
|
|
ENST00000438166.6:c.1928T>G
|
ENSP00000409708.2:p.Ile643Ser
|
|
ENST00000464846.5:n.366T>G
|
|
|
ENST00000492005.1:n.51T>G
|
|
|
ENST00000540309.5:c.*42T>G
|
ENSP00000440892.1:n.*42T>G
|
|
NM_000408.4:c.1928T>G
|
NP_000399.3:p.Ile643Ser
|
|
NM_001083112.2:c.1928T>G
|
NP_001076581.2:p.Ile643Ser
|
|
XM_005246469.1:c.1928T>G
|
XP_005246526.1:p.Ile643Ser
|
|
XM_005246470.3:c.1826T>G
|
XP_005246527.1:p.Ile609Ser
|
|
XM_011510977.1:c.1928T>G
|
XP_011509279.1:p.Ile643Ser
|
|
XM_011510978.1:c.1826T>G
|
XP_011509280.1:p.Ile609Ser
|
|
XM_011510979.1:c.1550T>G
|
XP_011509281.1:p.Ile517Ser
|
|
XM_011510980.1:c.1247T>G
|
XP_011509282.1:p.Ile416Ser
|
|
XM_005246469.2:c.1928T>G
|
XP_005246526.1:p.Ile643Ser
|
|
XM_011510977.2:c.1928T>G
|
XP_011509279.1:p.Ile643Ser
|
|
XM_011510978.2:c.1826T>G
|
XP_011509280.1:p.Ile609Ser
|
|
XM_017003830.1:c.1928T>G
|
XP_016859319.1:p.Ile643Ser
|
|
XM_024452798.1:c.1928T>G
|
XP_024308566.1:p.Ile643Ser
|
|
NM_000408.5:c.1928T>G
MANE Select
|
NP_000399.3:p.Ile643Ser
|
|
NM_001083112.3:c.1928T>G
|
NP_001076581.2:p.Ile643Ser
|
|