|
ENST00000685102.1:c.2359T>C
|
ENSP00000509257.1:p.Tyr787His
|
|
|
ENST00000685243.1:c.463T>C
|
ENSP00000508858.1:p.Tyr155His
|
|
|
ENST00000686270.1:c.2038T>C
|
ENSP00000509279.1:p.Tyr680His
|
|
|
ENST00000686339.1:c.1796-19T>C
|
ENSP00000510111.1:n.1796-19T>C
|
|
|
ENST00000686771.1:c.2047T>C
|
ENSP00000510484.1:p.Tyr683His
|
|
|
ENST00000686793.1:n.1543T>C
|
|
|
|
ENST00000686934.1:c.*1512T>C
|
ENSP00000510751.1:n.*1512T>C
|
|
|
ENST00000687202.1:n.4508T>C
|
|
|
|
ENST00000688122.1:n.4064T>C
|
|
|
|
ENST00000688235.1:n.3646T>C
|
|
|
|
ENST00000688943.1:n.3350T>C
|
|
|
|
ENST00000689366.1:n.4568T>C
|
|
|
|
ENST00000689677.1:n.2426T>C
|
|
|
|
ENST00000689853.1:c.*1512T>C
|
ENSP00000510653.1:n.*1512T>C
|
|
|
ENST00000689971.1:n.1237T>C
|
|
|
|
ENST00000690391.1:n.2693T>C
|
|
|
|
ENST00000690627.1:c.2107T>C
|
ENSP00000508820.1:p.Tyr703His
|
|
|
ENST00000690907.1:n.2912T>C
|
|
|
|
ENST00000691256.1:c.*3345T>C
|
ENSP00000510513.1:n.*3345T>C
|
|
|
ENST00000691404.1:c.2341T>C
|
ENSP00000509252.1:p.Tyr781His
|
|
|
ENST00000691682.1:c.2281T>C
|
ENSP00000509679.1:p.Tyr761His
|
|
|
ENST00000691813.1:c.*1155-19T>C
|
ENSP00000510547.1:n.*1155-19T>C
|
|
|
ENST00000692056.1:c.1996T>C
|
ENSP00000509505.1:p.Tyr666His
|
|
|
ENST00000692209.1:c.1912T>C
|
ENSP00000510201.1:p.Tyr638His
|
|
|
ENST00000692214.1:n.3664T>C
|
|
|
|
ENST00000692853.1:c.2095T>C
|
ENSP00000509649.1:p.Tyr699His
|
|
|
ENST00000692975.1:c.2281T>C
|
ENSP00000509892.1:p.Tyr761His
|
|
|
ENST00000693156.1:c.1978T>C
|
ENSP00000510144.1:p.Tyr660His
|
|
|
ENST00000400181.9:c.2353T>C
MANE Select
|
ENSP00000383042.5:p.Tyr785His
|
|
|
ENST00000465864.2:c.2299T>C
|
ENSP00000473297.2:p.Tyr767His
|
|
|
ENST00000356634.7:c.2281T>C
|
ENSP00000349049.3:p.Tyr761His
|
|
|
ENST00000400181.8:c.2353T>C
|
ENSP00000383042.4:p.Tyr785His
|
|
|
ENST00000494920.1:c.637T>C
|
ENSP00000473294.1:p.Tyr213His
|
|
|
ENST00000602503.1:n.1402T>C
|
|
|
|
NM_001009999.2:c.2353T>C
|
NP_001009999.1:p.Tyr785His
|
|
|
NM_015013.3:c.2281T>C
|
NP_055828.2:p.Tyr761His
|
|
|
XM_005245786.1:c.2341T>C
|
XP_005245843.1:p.Tyr781His
|
|
|
XM_006710472.2:c.2299T>C
|
XP_006710535.1:p.Tyr767His
|
|
|
XM_006710473.1:c.2359T>C
|
XP_006710536.1:p.Tyr787His
|
|
|
XM_006710474.2:c.2359T>C
|
XP_006710537.1:p.Tyr787His
|
|
|
NM_001363654.1:c.2299T>C
|
NP_001350583.1:p.Tyr767His
|
|
|
XM_005245786.2:c.2341T>C
|
XP_005245843.1:p.Tyr781His
|
|
|
XM_006710473.3:c.2359T>C
|
XP_006710536.1:p.Tyr787His
|
|
|
XM_006710474.3:c.2359T>C
|
XP_006710537.1:p.Tyr787His
|
|
|
XM_017000716.1:c.2341T>C
|
XP_016856205.1:p.Tyr781His
|
|
|
XM_017000717.1:c.2281T>C
|
XP_016856206.1:p.Tyr761His
|
|
|
NM_001009999.3:c.2353T>C
MANE Select
|
NP_001009999.1:p.Tyr785His
|
|
|
NM_001363654.2:c.2299T>C
|
NP_001350583.1:p.Tyr767His
|
|
|
NM_015013.4:c.2281T>C
|
NP_055828.2:p.Tyr761His
|
|
