ENST00000537320.6:c.3827C>G
|
ENSP00000443478.1:p.Ser1276Ter
|
|
ENST00000542877.6:c.4649C>G
|
ENSP00000442242.1:p.Ser1550Ter
|
|
ENST00000705190.1:c.2681C>G
|
ENSP00000516083.1:p.Ser894Ter
|
|
ENST00000705191.1:c.1337C>G
|
ENSP00000516084.1:p.Ser446Ter
|
|
ENST00000705192.1:c.4696C>G
|
|
|
ENST00000350763.9:c.5738C>G
MANE Select
|
ENSP00000265131.4:p.Ser1913Ter
|
|
ENST00000341037.8:c.5192C>G
|
ENSP00000339553.4:p.Ser1731Ter
|
|
ENST00000350763.8:c.5738C>G
|
ENSP00000265131.4:p.Ser1913Ter
|
|
ENST00000423613.6:c.4919C>G
|
ENSP00000411406.2:p.Ser1640Ter
|
|
ENST00000460345.1:n.320C>G
|
|
|
ENST00000535648.5:c.4649C>G
|
ENSP00000438152.2:p.Ser1550Ter
|
|
ENST00000537320.5:c.3827C>G
|
ENSP00000443478.1:p.Ser1276Ter
|
|
ENST00000542877.5:c.4649C>G
|
ENSP00000442242.1:p.Ser1550Ter
|
|
ENST00000544972.1:c.1425C>G
|
|
|
NM_002160.3:c.5738C>G
|
NP_002151.2:p.Ser1913Ter
|
|
XM_005251972.2:c.5465C>G
|
XP_005252029.1:p.Ser1822Ter
|
|
XM_005251973.2:c.4646C>G
|
XP_005252030.1:p.Ser1549Ter
|
|
XM_005251974.2:c.4100C>G
|
XP_005252031.1:p.Ser1367Ter
|
|
XM_005251975.2:c.3827C>G
|
XP_005252032.1:p.Ser1276Ter
|
|
XM_006717096.2:c.6014C>G
|
XP_006717159.1:p.Ser2005Ter
|
|
XM_006717097.2:c.5465C>G
|
XP_006717160.1:p.Ser1822Ter
|
|
XM_006717098.2:c.5192C>G
|
XP_006717161.1:p.Ser1731Ter
|
|
XM_006717100.2:c.4919C>G
|
XP_006717163.1:p.Ser1640Ter
|
|
XM_006717101.2:c.4100C>G
|
XP_006717164.1:p.Ser1367Ter
|
|
XM_011518622.1:c.5741C>G
|
XP_011516924.1:p.Ser1914Ter
|
|
XM_011518623.1:c.5741C>G
|
XP_011516925.1:p.Ser1914Ter
|
|
XM_011518624.1:c.5195C>G
|
XP_011516926.1:p.Ser1732Ter
|
|
XM_011518625.1:c.5192C>G
|
XP_011516927.1:p.Ser1731Ter
|
|
XM_011518626.1:c.4922C>G
|
XP_011516928.1:p.Ser1641Ter
|
|
XM_011518627.1:c.4649C>G
|
XP_011516929.1:p.Ser1550Ter
|
|
XM_011518628.1:c.4373C>G
|
XP_011516930.1:p.Ser1458Ter
|
|
XM_011518629.1:c.4373C>G
|
XP_011516931.1:p.Ser1458Ter
|
|
XM_005251972.4:c.5465C>G
|
XP_005252029.1:p.Ser1822Ter
|
|
XM_005251973.4:c.4646C>G
|
XP_005252030.1:p.Ser1549Ter
|
|
XM_005251974.4:c.4100C>G
|
XP_005252031.1:p.Ser1367Ter
|
|
XM_005251975.4:c.3827C>G
|
XP_005252032.1:p.Ser1276Ter
|
|
XM_006717096.4:c.6014C>G
|
XP_006717159.1:p.Ser2005Ter
|
|
XM_006717097.4:c.5465C>G
|
XP_006717160.1:p.Ser1822Ter
|
|
XM_006717098.4:c.5192C>G
|
XP_006717161.1:p.Ser1731Ter
|
|
XM_006717101.4:c.4100C>G
|
XP_006717164.1:p.Ser1367Ter
|
|
XM_011518625.3:c.5192C>G
|
XP_011516927.1:p.Ser1731Ter
|
|
XM_011518626.3:c.4922C>G
|
XP_011516928.1:p.Ser1641Ter
|
|
XM_011518628.3:c.4373C>G
|
XP_011516930.1:p.Ser1458Ter
|
|
XM_011518629.3:c.4373C>G
|
XP_011516931.1:p.Ser1458Ter
|
|
XM_017014678.2:c.6287C>G
|
XP_016870167.1:p.Ser2096Ter
|
|
XM_017014679.2:c.6014C>G
|
XP_016870168.1:p.Ser2005Ter
|
|
XM_017014680.2:c.6011C>G
|
XP_016870169.1:p.Ser2004Ter
|
|
XM_017014681.2:c.5195C>G
|
XP_016870170.1:p.Ser1732Ter
|
|
XM_024447530.1:c.6287C>G
|
XP_024303298.1:p.Ser2096Ter
|
|
NM_002160.4:c.5738C>G
MANE Select
|
NP_002151.2:p.Ser1913Ter
|
|